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

22 catalysts · 8 device recall · 7 device pma · 6 device 510k · 1 approval

★ save view↓export CSV
next 91 dayslessmore
MonWedFri
2026-08-10: 75 catalysts2026-08-11: 16 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: 2 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: 20 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 8 catalysts2026-11-03: 17 catalysts2026-11-04: 22 catalysts2026-11-05: 36 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
view
agendamonth
sort
soonestlatesttypesponsoralpha
from 2025-08-04×to 2025-08-04×clear all
type
  • device recall8
  • device pma7
  • device 510k6
  • approval1
therapy area

no tagged catalysts yet

Week of Aug 4, 2025

22
›
Aug 4, 2025
approval
372d ago
OXYCODONE HYDROCHLORIDE — FDA approvalOXYCODONE HYDROCHLORIDE

Sponsor: ASCENT PHARMS INC. Form: TABLET. Route: ORAL

full page →OXYCODONE HYDROCHLORIDE →fda approvals ↗
›Aug 4, 2025device pma372d agoAcu Focus, Inc. — IC-8 Apthera Intraocular Lens (IOL) (PMA supplement)

Supplement type: Special (Immediate Track). Product code: POE. Advisory committee: OP. Decision: APPR

full page →fda device pma ↗
›Aug 4, 2025device pma372d agoOxford Immunotec, Ltd. — T-SPOT.TB TEST (PMA supplement)

Supplement type: Real-Time Process. Product code: OJN. Advisory committee: MI. Decision: APPR

full page →fda device pma ↗
›Aug 4, 2025device pma372d agoABBOTT MEDICAL — Avant (CDHFA700Q, CDHFA700T); Neutrino NxT (CDHFA800Q, CDHFA800T CDHFA600Q, CDHFA600T); Gallant (CDHFA500Q, CDHFA500T); (PMA supplement)

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

full page →fda device pma ↗
›Aug 4, 2025device pma372d agoSiemens Healthcare Diagnostics Products, Ltd. — IMMULITE 2000 Systems Total Antibodies to Hepatitis B Core Antigen (Anti-HBc) (PMA supplement)

Supplement type: 30-Day Notice. Product code: LOM. Advisory committee: MI. Decision: OK30

full page →fda device pma ↗
›Aug 4, 2025device pma372d agoABBOTT MEDICAL — Avant™ VR (CDVRA700Q, CDVRA700T); Neutrino™ NxT VR (CDVRA800Q, CDVRA800T CDVRA600Q, CDVRA600T); Gallant™ VR (CDVRA500Q, (PMA supplement)

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

full page →fda device pma ↗
›Aug 4, 2025device pma372d agoAgilent Technologies, Inc. — PD-L1 IHC 22C3 pharmDx (Dako Omnis) (PMA supplement)AGILENT TECHNOLOGIES, INC.

Supplement type: Normal 180 Day Track. Product code: PLS. Advisory committee: PA. Decision: APPR

full page →fda device pma ↗
›Aug 4, 2025device pma372d agoOxford Immunotec, Ltd. — T-SPOT.TB Test (PMA supplement)

Supplement type: 30-Day Notice. Product code: OJN. Advisory committee: MI. Decision: OK30

full page →fda device pma ↗
›Aug 4, 2025device recall372d agoWASATCH PHOTONICS device recall (Cls II)

Wasatch Photonics 785/830-SR and 785-ER-ILC Raman Spectrometers, Product Models: 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC,785-ER-ILC. — Reason: Two new potential laser safety failure modes have been identified in the product design. Overcurrent of laser diode, and a fail-unsafe mode. The failure modes have never been found to occur in these models, whether in the field or factory, but could potentially occur under excessive force or extreme, continuous vibration. — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device recall372d agoBaxter Healthcare Corporation device recall (Cls I)Baxter Healthcare Corp

Novum IQ Syringe Pump, Product Code 40800BAXUS, infusion pump — Reason: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only). — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device recall372d agoAVID Medical, Inc. device recall (Cls II)AVITA Medical, Inc.

Halyard, ENT PACK. Model Number: JACK421-04. Convenience kit. — Reason: Potential for open header bag seals, compromising sterility. — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device recall372d agoBaxter Healthcare Corporation device recall (Cls I)Baxter Healthcare Corp

Novum IQ LVP (Large Volume Pump), Product Code 40700BAXUS, infusion pump — Reason: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only). — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device recall372d agoBeckman Coulter Inc. device recall (Cls II)

DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clinical Analyzer — Reason: On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the CC tests, CC sample status will remain In Progress with no errors, may cause processing delays. — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device recall372d agoBaxter Healthcare Corporation device recall (Cls I)Baxter Healthcare Corp

Novum IQ Syringe Pump, Product Code 40700BAX, infusion pump — Reason: Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction for the Novum IQ Large Volume Pump (LVP) and Novum IQ Syringe Pump (SP) due to software anomalies that may result in a blank Run screen (LVP and SP) and/or false motor movement system error (SP only). — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device recall372d agoAVID Medical, Inc. device recall (Cls II)AVITA Medical, Inc.

Halyard, CPT BASIC IR PACK. Model Number: 1646381. Convenience kit. — Reason: Potential for open header bag seals, compromising sterility. — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device recall372d agoMerit Medical Systems, Inc. device recall (Cls II)MERIT MEDICAL SYSTEMS INC

PhD Hemostasis Valve, REF: IN4802/K, IN4802/T, IN4918/A, IN7802/C, IN8802/C, IN9802, IN9802/A, K05-02166B, K05T-02138A, K12T-10798A, MAP800/B, MAP800/T, MAP801/B, MAP802/B, MAP802/CNB, MAP802/T, MAP804/B, MAP852/B, SKY1802. — Reason: Hemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in procedure inconvenience and/or hemorrhage. — Status: Ongoing

full page →fda device recalls ↗
›Aug 4, 2025device 510k372d agoTerragene — Terragene® Bionova® BT20 Biological Indicator (510k cleared)

Product code: FRC. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Aug 4, 2025device 510k372d agoSpectrum Medical S.R.L. — Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG) (510k cleared)

Product code: KFM. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Aug 4, 2025device 510k372d agoAndon Health Co, Ltd. — iHealth Compare Wireless Blood Pressure Monitor(BP-300C);iHealth Compare Pro Wireless Blood Pressure Monitor(BP-300CV);iHealth Compare S Wireless Blood Pressure Monitor(BP-300V);iHealth Wireless Blood Pressure Monitor(BPX1);iHealth Blood Pressure Monitor(KD-595);iHealth Track Pro Connected Blood Pressure Monitor(KN-550LT);Semi Automatic Blood Pressure Monitor(KD-388N);Arm Blood Pressure Monitor(KD-553);Arm Blood Pressure Monitor(KD-557BR);Arm Blood Pressure Monitor(KD-558);Arm Blood Pr (510k cleared)

Product code: DXN. Advisory committee: Cardiovascular. Type: Abbreviated

full page →fda device 510k ↗
›Aug 4, 2025device 510k372d agoOkapi Medical, LLC Dba Resivant Medical — CUTIVA™ Topical Skin Adhesive (RM1700); CUTIVA™ PLUS Skin Closure System (RM1739) (510k cleared)

Product code: MPN. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Aug 4, 2025device 510k372d agoDaxor Corporation — Blood Volume Analyzer (200) (510k cleared)DAXOR CORP

Product code: JWO. Advisory committee: Hematology. Type: Traditional

full page →fda device 510k ↗
›Aug 4, 2025device 510k372d agoH&abyz Co., Ltd. — HnX-P1, HnX-PB (510k cleared)

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

full page →fda device 510k ↗
$MMSI89.75+0.80%
$RCEL7.6000-2.19%
$RCEL7.6000-2.19%
$A148.72+1.88%
$DXR