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19,210 catalysts · 4,728 grant · 3,230 8k filing · 2,681 approval · 2,496 device 510k · 2,000 device recall · 1,747 device pma

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2026-08-10: 0 catalysts2026-08-11: 0 catalysts2026-08-12: 0 catalysts2026-08-13: 60 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
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  • grant4,728
  • 8k filing3,230
  • approval2,681
  • device 510k2,496
  • device recall2,000
  • device pma1,747
  • device adverse event1,000
  • recall663
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jun 30, 2025

    50
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    3D6-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    C9-4v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    S3-1 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    S8-3t Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    D5cwc Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    Transducer C10-3v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    X11-4t Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    L12-3 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    Mini Multi TEE Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    S4-1 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    c5-1 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    V6-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    C9-4 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    L12-5 50 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    V9-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    XL14-3 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    X8-2t Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    C9-3io Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    L11-3 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    OMNI III TEE Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoOrascoptic Surgical Acuity device recall (Cls II)

    Orascoptic Superior Visualization Custom loupes with Dragonfly frames — Reason: Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    D2TCD Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    C5-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    L15-7IO TRANSDUCER Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    X7-2t Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoOrascoptic Surgical Acuity device recall (Cls II)

    Orascoptic Superior Visualization Custom loupes configured with Phantom Frames — Reason: Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    L17-5 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    C10-3v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoOrascoptic Surgical Acuity device recall (Cls II)

    Orascoptic Superior Visualization Phantom Essential kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver) — Reason: Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    C9-5ec Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    S8-3 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    S12-4 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    S7-2t Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall407d agoPhilips Ultrasound, Inc device recall (Cls III)

    X3-1 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device 510k407d agoTherapixel — MammoScreen® (4) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoSiemens Medical Solutions USA, Inc. — SOMATOM go.Now; SOMATOM go.Up; SOMATOM go.All; SOMATOM go.Top; SOMATOM go.Sim; SOMATOM go.Open Pro; SOMATOM Pro.Pulse (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoBoston Scientific — Advanix™ Pancreatic Stent and NaviFlex™ Rapid Exchange (RX) Pancreatic Delivery System and Pushers (510k cleared)BOSTON SCIENTIFIC CORP

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoLima Corporate S.P.A. — SMR Reverse HP Shoulder System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoHunan Vathin Medical Instrument Co., Ltd. — Single-use Ureteral Access Sheath (510k cleared)

    Product code: FED. Advisory committee: Gastroenterology, Urology. Type: Special

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoGuangzhou Pinzhi Medical Device Co., Ltd. — Denudation Pipettes (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoWontech Co., Ltd. — Pastelle (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoThe Magstim Company Limited — Rapid2 Magnetic Stimulators (Magstim Rapid2, Magstim Super Rapid2, Magstim Super Rapid2 Plus1) (510k cleared)

    Product code: QPL. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoW&H Dentalwerk Buermoos GmbH — Piezomed Pro (Piezomed Pro module M-PM100 incl. handpiece M-PH350, Piezomed Pro instruments (various tips) and accessories) (510k cleared)

    Product code: ERL. Advisory committee: Ear, Nose, Throat. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoAveera Medical, Inc. — Boomerang Valvulotome (BMGVT080); Boomerang Push Valvulotome (BMGPVT125) (510k cleared)AVITA Medical, Inc.

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoBioventus, LLC — TalisMann Neuromodulation System (510k cleared)Bioventus Inc.

    Product code: GZF. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoBimed Teknik Aletler Sanayi & Ticaret A.S. — 3DOSE 1ml Syringe (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoSiemens Medical Solutions USA, Inc. — Biograph Vision PET/CT Systems; Biograph mCT PET/CT Systems (510k cleared)

    Product code: KPS. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoTruabutment, Inc. — URIS Long Implant & Abutments (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoBecton, Dickinson and Company — BD Vacutainer® Eclipse™ Blood Collection Needle (510k cleared)BECTON DICKINSON & CO

    Product code: JKA. Advisory committee: Clinical Chemistry. Type: Traditional

    full page →fda device 510k ↗
    ›Jul 3, 2025device 510k407d agoAlphatec Spine, Inc. — IdentiTi II Cervical Interbody System (510k cleared)

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

    full page →fda device 510k ↗
    ← prev
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    $BSX51.39-0.07%
    $BDX182.19-0.76%
    $BVS8.6700+1.40%
    $RCEL8.5389+5.16%