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9,503 catalysts · 3,332 8k filing · 2,032 grant · 1,000 device adverse event · 910 approval · 674 device 510k · 584 earnings

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  • 8k filing3,332
  • grant2,032
  • device adverse event1,000
  • approval910
  • device 510k674
  • earnings584
device pma
508
  • device recall215
  • phase 2 completion172
  • recall167
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Feb 23, 2026

    50
    ›Feb 25, 2026device 510k171d agoMedline Industries, LP — Konig Bell Circumcision Clamp (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k171d agoGrindguard, Inc. — Remi Impression Material (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k171d agoMako Surgical Corp. — Mako Total Knee Application (510k cleared)

    Product code: OLO. Advisory committee: Neurology. Type: Special

    full page →fda device 510k ↗
    ›Feb 25, 2026device 510k171d agoMighty Oak Medical — FIREFLY® Pedicle Screw Navigation Guide (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 25, 2026device pma171d agoNovocure, GmbH — Optune Gio® (PMA supplement)NovoCure Ltd

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

    full page →fda device pma ↗
    ›Feb 25, 2026device pma171d agoBoston Scientific Corporation — Axonics Sacral Neuromodulation System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: EZW. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device pma171d agoBoston Scientific Corporation — Axonics Sacral Neuromodulation System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: QON. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device pma171d agoABBOTT MEDICAL — TriClip™ G5 Delivery System (TCDS0801-NT, TCDS0801-NTW, TCDS0801-XT, TCDS0801-XTW) (PMA supplement)

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

    full page →fda device pma ↗
    ›Feb 25, 2026device pma171d agoIntegra Lifesciences Corp. — INTEGRA ® Dermal Regeneration Template; Integra® Meshed Dermal Regeneration Template; Integra® Omnigraft Dermal Regenera (PMA supplement)INTEGRA LIFESCIENCES HOLDINGS CORP

    Supplement type: 30-Day Notice. Product code: MGR. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device pma171d agoABBOTT MEDICAL — MitraClip™ G5 Delivery System (CDS0801-NT, CDS0801-NTW, CDS0801-XT, CDS0801-XTW) (PMA supplement)

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

    full page →fda device pma ↗
    ›Feb 25, 2026device pma171d agoNovocure, GmbH — Optune Lua® (PMA supplement)NovoCure Ltd

    Supplement type: 30-Day Notice. Product code: SDA. Advisory committee: AN. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device pma171d agoBoston Scientific Corp — AMS 800™ Artificial Urinary Sphincter (AUS) (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: EZY. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Feb 25, 2026device recall171d agoSynthes (USA) Products LLC device recall (Cls II)

    2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US. — Reason: A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 3005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus PKS Cutting Forceps w/Cord, 5mm 24cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920000PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation during an endoscopic or open surgical procedure. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus Everest Bipolar Cutting Forceps, 5 mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3005 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the bipolar outputs of compatible generators. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3006 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the bipolar outputs of compatible generators. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus PKS Cutting Forceps, 5mm 33cm Product Name: PKS Cutting Forceps Model/Catalog Number: 920005PK Product Description: The PKS Cutting Forceps are intended to be passed through a 5mm cannula. Coagulation is achieved using electrosurgical energy under visualization. The device is intended to be used with the PKS electrical generator. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: Olympus HALO PKS Cutting Forceps, 5mm 33cm Product Name: HALO PKS Cutting Forceps Model/Catalog Number: HACF0533 Product Description: The HALO PKS Cutting Forceps are intended to be passed through a 5 mm laparoscopic cannula. Coagulation is achieved using electrosurgical energy under laparoscopic visualization. The device is intended to be used with the Gyrus ACMI G400 Workstation only. — Reason: Olympus identified that the Cutting Forceps contain components for which the supplier did not adequately validate the welding process. Defective welds can result in the Cutting Forceps' jaw breaking during clinical use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026device recall171d agoSynthes (USA) Products LLC device recall (Cls II)

    2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM. Part Number: 03.424.126-US. — Reason: A full lot swap between VOLT Locking Screw Tap 03.424.124 lot 68900P9 and Cortical Screw Tap 03.424.126 lot 68982P8, resulting in the bones taps having an incorrect thread. — Status: Ongoing

    full page →fda device recalls ↗
    ›Feb 25, 2026grant171d agoHENRY FORD HEALTH + MICHIGAN STATE UNIVERSITY HEALTH SCIENCES — Advancing Cardiovascular Health Among Adolescents with Intellectual Disabilit...

    NR grant. $169,189. PI: Patricia Marie West

    full page →nih reporter ↗
    ›Feb 25, 2026grant171d agoUNIVERSITY OF COLORADO DENVER — Understanding the contributions of MAIT cells in colitisUniversity of Colorado Denver

    AI grant. $429,000. PI: Li Yen Loh

    full page →nih reporter ↗
    ›Feb 25, 2026grant171d agoKEYSTONE SYMPOSIA — B and T Cell Collaboration in Lymphoid and Nonlymphoid Microenvironments

    AI grant. $14,000. PI: TERRY L. SHEPPARD

    full page →nih reporter ↗
    ›Feb 25, 2026grant171d agoKEYSTONE SYMPOSIA — B Cells and Plasma Cells: Fundamental and Translational Biology

    AI grant. $15,500. PI: TERRY L. SHEPPARD

    full page →nih reporter ↗
    ›Feb 25, 2026grant171d agoFLORIDA STATE UNIVERSITY — Multi-level factors influencing maternal and infant health outcomes

    HD grant. $540,915. PI: Patricia Ann Homan

    full page →nih reporter ↗
    ›Feb 25, 2026grant171d agoMAYO CLINIC JACKSONVILLE — Role of meningeal lymphatic drainage in CSF1R-related leukoencephalopathyMayo Clinic

    NS grant. $50,114. PI: Guadalupe Sanchez

    full page →nih reporter ↗
    ›Feb 26, 2026approval170d agoXeomin (incobotulinumtoxinA) — FDA approvalMerz Pharmaceuticals LLC

    Sponsor: MERZ PHARMS. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Feb 26, 2026approval170d agoDAPSONE — FDA approvalDAPSONE

    Sponsor: ZYDUS LIFESCIENCES. Form: TABLET. Route: ORAL

    full page →DAPSONE →fda approvals ↗
    ›Feb 26, 2026approval170d agoJASCAYD (NERANDOMILAST) — FDA approvalnerandomilast

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

    full page →nerandomilast →fda approvals ↗
    ›Feb 26, 2026approval170d agoVYVGART HYTRULO (EFGARTIGIMOD ALFA AND HYALURONIDASE-QVFC) — FDA approvalARGENX SE

    Sponsor: ARGENX BV. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Feb 26, 2026approval170d agoBUMETANIDE — FDA approvalEdenbridge Pharmaceuticals LLC

    Sponsor: ANTHEA PHARMA. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Feb 26, 2026approval170d agoPHYTONADIONE — FDA approvalPHYTONADIONE

    Sponsor: SINOTHERAPEUTICS INC. Form: TABLET. Route: ORAL

    full page →PHYTONADIONE →fda approvals ↗
    ›Feb 26, 2026approval170d agoONDANSETRON HYDROCHLORIDE — FDA approvalRedHill Biopharma Ltd.

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Feb 26, 2026approval170d agoONDANSETRON HYDROCHLORIDE — FDA approvalRedHill Biopharma Ltd.

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Feb 26, 2026approval170d agoHERNEXEOS (ZONGERTINIB) — FDA approvalzongertinib

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

    full page →zongertinib →fda approvals ↗
    ›Feb 26, 2026approval170d agoRIZAFILM (RIZATRIPTAN BENZOATE) — FDA approvalNAL Pharmaceuticals Ltd

    Sponsor: GENSCO. Form: FILM. Route: ORAL

    full page →fda approvals ↗
    ›Feb 26, 2026approval170d agoDALBAVANCIN HYDROCHLORIDE — FDA approvalLong Grove Pharmaceuticals LLC

    Sponsor: LONG GROVE PHARMS. Form: POWDER. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Feb 26, 2026approval170d agoENSACOVE (ENSARTINIB HYDROCHLORIDE) — FDA approvalensartinib hydrochloride

    Sponsor: XCOVERY. Form: CAPSULE. Route: ORAL

    full page →ensartinib hydrochloride →fda approvals ↗
    ›Feb 26, 2026approval170d agoPHYTONADIONE — FDA approvalPHYTONADIONE

    Sponsor: BAXTER HLTHCARE CORP. Form: INJECTABLE. Route: INJECTION

    full page →PHYTONADIONE →fda approvals ↗
    ›Feb 26, 2026approval170d agoIVERMECTIN — FDA approvalIVERMECTIN

    Sponsor: ZYDUS LIFESCIENCES. Form: TABLET. Route: ORAL

    full page →IVERMECTIN →fda approvals ↗
    ›Feb 26, 2026device 510k170d agoSibel Health, Inc. — ANNE Maternal (510k cleared)Seed Health Inc

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoGlobus Medical, Inc. — RIB LINK™ Fixation System (510k cleared)GLOBUS MEDICAL INC

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoORO Co., Ltd. — CAPRI (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoOsteonic Co., Ltd. — Aster (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoImplanet — SWINGO-3D Lumbar Cage System (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoMedacta International S.A. — GMK 3D Metal Tibial Tray Extension (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoKarl Storz SE & CO. KG — KARL STORZ ICG Imaging System with RUBINA® Lens (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoShanghai AnQing Medical Instrument Co., Ltd. — InnovexView (GC146-17, GC150-20, GC155-23) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2026device 510k170d agoAidoc Medical , Ltd. — BriefCase-Triage: CARE Multi-Triage CT for Pneumothorax; Pericardial effusion; Large aortic aneurysm; Shoulder fracture or dislocation device (510k cleared)

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

    full page →fda device 510k ↗
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    $IART18.240.00%
    $BSX52.44+1.44%
    $BSX52.44+1.44%
    $BSX52.44+1.44%
    $NVCR20.05+28.74%
    $NVCR20.05+28.74%
    $ARGX844.92-1.40%
    $SIGY0.04000.00%
    $RDHL0.7390+6.64%
    $RDHL0.7390+6.64%
    $GMED79.93+1.27%