pharmadog
News
when
  • Latest
  • Archive
by source
  • All Sources
  • Sources Page
Jobs
department
  • Clinical
  • Regulatory
  • Medical Affairs
  • Commercial
  • R&D / Discovery
  • Biostatistics / Data
  • Manufacturing / CMC
  • Market Access
therapeutic area
  • Oncology
  • Immunology
  • Neuroscience
  • Cardiovascular
  • Metabolic
  • Rare Disease
  • Infectious Disease
location & type
  • Remote Only
  • US Only
  • California
  • Massachusetts
  • Internships
  • Phase 3 Roles
  • All Jobs →
Sign InSubscribe
pharmadog

fetch the data · sniff the signal

Discover
  • Jobs
  • News
Hubs
  • Topics
  • Patent cliff
  • Publications
Tools
  • Compare
  • Search
  • Bookmarks
Trust
  • About
  • Sources
  • Contact
Legal
  • Privacy
  • Terms
  • Pricing

© 2026 pharmadog.xyz

made by humans and a good dog

  • home
  • jobs
  • news
  • search

calendar

18,200 catalysts · 4,728 grant · 3,126 8k filing · 2,634 approval · 2,175 device 510k · 1,759 device recall · 1,520 device pma

★ save view↓export CSV
next 91 dayslessmore
MonWedFri
2026-08-10: 0 catalysts2026-08-11: 0 catalysts2026-08-12: 19 catalysts2026-08-13: 19 catalysts2026-08-14: 4 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 3 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 1 catalyst2026-08-27: 1 catalyst2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
view
agendamonth
sort
soonestlatesttypesponsoralpha
from 2025-08-06×clear all
type
  • grant4,728
  • 8k filing3,126
  • approval2,634
  • device 510k2,175
  • device recall1,759
  • device pma1,520
device adverse event
1,000
  • recall593
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Aug 18, 2025

    50
    ›Aug 20, 2025device pma357d agoABBOTT MEDICAL — TriClip G5 Delivery System (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: NPS. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoCooperVision, Inc. — iWear oxygen presbyopia (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: LPM. Advisory committee: OP. Decision: APPR

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoMedtronic Minimed, Inc. — MiniMed 770G System (PMA supplement)Medtronic USA Inc

    Supplement type: Normal 180 Day Track No User Fee. Product code: OZP. Advisory committee: CH. Decision: APPR

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoAdvanced Bionics — HiResolution™ Bionic Ear System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MCM. Advisory committee: EN. Decision: OK30

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoOrganox Limited — OrganOx metra® System (PMA supplement)

    Supplement type: Real-Time Process. Product code: QQK. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoStryker Neurovascular — Surpass Streamline Flow Diverter (PMA supplement)

    Supplement type: 30-Day Notice. Product code: OUT. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoElement Science, Inc. — Jewel Patch Wearable Cardioverter Defibrillator (P-WCD) (Jewel), Jewel P-WCD Firmware, Device Accessories Skin Preparati (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: MVK. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoCarl Zeiss Meditec Production, LLC — CT LUCIA 602; CT LUCIA 202; CT LUCIA 611P; CT LUCIA 621P (PMA supplement)

    Supplement type: 30-Day Notice. Product code: HQL. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoW. L. Gore & Associates, Inc. — GORE® EXCLUDER® AAA Endoprosthesis (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MIH. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoMedtronic, Inc. — MEDTRONIC MICRA TRANSCATHETER PACEMAKER SYSTEM (PMA supplement)Medtronic plc

    Supplement type: Real-Time Process. Product code: PNJ. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoABBOTT MEDICAL — MitraClip G5 Delivery System (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: NKM. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 20, 2025device pma357d agoAtrium Medical Corp. — iCast Covered Stent System (PMA supplement)Apyx Medical Corp

    Supplement type: 30-Day Notice. Product code: PRL. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L211 PROPONENT DR SL MRI Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number S702, ALTRUA 2 DR SL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number U128, VALITUDE CRT-P EL MRI — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoAbiomed, Inc. device recall (Cls I)Abion Inc

    Automated Impella Controller (AIC) with the below brands and product codes. Used with heart assist pump. 1. Impella Controller, Packaged, US; Product Code: 0042-0000-US. 2. Impella Controller, Packaged, US, Loaner; Product Code: 0042-0000-US-L. 3. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 4. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 5. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK. 6. Impella Controller, UK, Loaner; Product Code: 0042-0000-UK-L. — Reason: Specific Automated Impella Controllers (AICs) that have a Pump Driver Circuit Assembly do not meet current specifications. This may lead to decreased pump performance or pump stop and trigger an Impella Failure or Impella Stopped Controller Failure alarm. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L231, PROPONENT DR EL MRI Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L101, ESSENTIO DR SL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L209 PROPONENT DR (VDD) SL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number U226, VISIONIST CRT-P EL — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    PROPONENT SR SL (Model L200) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number U228, VISIONIST CRT-P EL MRI — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L221 PROPONENT DR EL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L131, ESSENTIO DR EL MRI Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    ACCOLADE DR EL MRI (Model L331) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoMicroSurgical Technology Inc device recall (Cls II)MICRON TECHNOLOGY INC

    MST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48-1000-01 — Reason: An ophthalmic knife has a suction set (not direct patient-contacting), which contains springs contaminated with an unidentified residue that may potentially cause eye irritation — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L121 ESSENTIO DR EL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L110, ESSENTIO SR SL MRI Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number U225 VISIONIST CRT-P EL — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L210 PROPONENT SR SL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    ACCOLADE DR SL (Model L301) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    ACCOLADE DR EL (Model L321) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number S701 ALTRUA 2 SR SL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L111, ESSENTIO DR SL MRI Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    ACCOLADE SR SL (Model L300) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number U125, VALITUDE CRT-P EL — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number L100, ESSENTIO SR SL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    ACCOLADE SR SL MRI (Model L310) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    PROPONENT DR SL (Model L201) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    Model Number S722, ALTRUA 2 DR EL Pacemaker — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device recall357d agoBoston Scientific Corporation device recall (Cls I)BOSTON SCIENTIFIC CORP

    ACCOLADE DR SL MRI (Model L311) — Reason: Software to enhance Safety Architecture is available and designed to prevent initiation of Safety Mode in an ambulatory setting due to a high battery impedance state for the ACCOLADE family of devices which includes ACCOLADE, PROPONENT, ESSENTIO, and ALTRUA 2 dual chamber (DR) standard life (SL) and DR extended life (EL) pacemakers; and VISIONIST and VALITUDE cardiac resynchronization therapy pacemakers (CRT-Ps). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 20, 2025device 510k357d agoBeckman Coulter, Inc. — MicroScan Dried Gram-Negative MIC/Combo Panels with Cefepime (CPE) (0.12-64 µg/mL) (MicroScan) (510k cleared)

    Product code: LTT. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoShenzhen TPH Technology Co., Ltd. — Wearable Breast Pump (Model W6) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoLiofilchem s.r.l. — MTS Sulbactam-Durlobactam 0.004/4 - 64/4 µg/mL (SUD) (510k cleared)

    Product code: JWY. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoTriMed, Inc. — Distal Xtremities System (510k cleared)

    Product code: HRS. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoStryker GmbH — T2 Alpha Humerus Nailing System; IMN Screws System; T2 Nailing System (510k cleared)STRYKER CORP

    Product code: HSB. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoZest Anchors, LLC — LOCATOR® Angled Abutment (510k cleared)

    Product code: NHA. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoSoftac Medical Technologies — EndoFix™Tissue Fixation System (510k cleared)Samson Medical Technologies LLC

    Product code: FGE. Advisory committee: Gastroenterology, Urology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoWondfo USA Co, Ltd. — WELLlife Flu A&B Home Test; WELLlife Influenza A&B Test (510k cleared)

    Product code: SCA. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 20, 2025device 510k357d agoMethinks Software, S.L — Methinks CTA Stroke (510k cleared)

    Product code: QAS. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ← prev
    page 8 of 364
    next →
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $MDT90.68+1.42%
    $APYX
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $MU868.52+0.87%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $FRTRY
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $BSX51.19+1.45%
    $SYK348.15+0.68%