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13,283 catalysts · 3,603 8k filing · 2,377 grant · 2,049 approval · 1,383 device 510k · 1,000 device adverse event · 930 device pma

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  • 8k filing3,603
  • grant2,377
  • approval2,049
  • device 510k1,383
  • device adverse event1,000
  • device pma930
device recall
912
  • earnings585
  • recall364
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 17, 2025

    50
    ›Nov 19, 2025device 510k283d agoShenzhen Dachi Communication Co., Ltd. — Microcurrent Facial Device (CEC101, EEI101) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k283d agoEdap Technomed, Inc. — Focal One® (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k283d agoGu'An Yeolight Smart Electronics Co., Ltd. — IPL Hair Removal Device (SYL001AZ, SYL002AZ) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k283d agoHuizhou Foryou Medical Devices Co., Ltd. — LUOFUCON® Skin and Wound Cleanser (Spray, Mist, Squeeze, Bottle.) (510k cleared)

    Product code: FRO. Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k283d agoSunglor Technology Co., Ltd. — LED Light Therapy Device (SG-FSM, SG-NK, SG-CT) (510k cleared)Viomi Technology Co., Ltd

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k283d agoVarian Medical Systems — Guided Aarhus Applicator Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device pma283d agoLife Technologies Corporation — Oncomine Dx Target Test (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 19, 2025device pma283d agoEdwards Lifesciences, LLC — EVOQUE Tricuspid Valve Replacement System (PMA supplement)Edwards Lifesciences Corp

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

    full page →fda device pma ↗
    ›Nov 19, 2025device pma283d 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 ↗
    ›Nov 19, 2025device pma283d agoImpulse Dynamics (Usa), Inc. — OPTIMIZER SMART Mini IPG (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: QFV. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Nov 19, 2025device pma283d agoSyncardia Systems, LLC — Total Artificial Heart (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: LOZ. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Nov 19, 2025device recall283d agoSteris Corporation device recall (Cls II)STERIS plc

    AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps and clamps), utensils (such as bedpans, urinals, trays, bowl, basin and kidney dishes), rubber and plastic goods, theatre shoes and other similar and related articles found in healthcare facilities. — Reason: Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users). — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 19, 2025device recall283d agoSteris Corporation device recall (Cls II)STERIS plc

    AMSCO 7053HP Washer/Disinfector Model/Catalog Number: 7053HP Product Description: The AMSCO 7053HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps and clamps), utensils (such as bedpans, urinals, trays, bowl, basin and kidney dishes), rubber and plastic goods, theatre shoes and other similar and related articles found in healthcare facilities. — Reason: Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains internal within the unit (no risk of shock to users). — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 19, 2025device recall283d agoVortex Surgical Inc. device recall (Cls II)

    Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25; — Reason: Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 19, 2025grant283d agoUNIVERSITY OF NEW MEXICO HEALTH SCIS CTR — The Role of Iron in Pulmonary Arterial Hypertension-Associated NeurodegenerationSri Devaraj Urs Academy of Higher Education and Research

    GM grant. $259,250. PI: Priscilla Marie De La Cruz

    full page →nih reporter ↗
    ›Nov 20, 2025approval282d agoPALYNZIQ (PEGVALIASE-PQPZ) — FDA approvalBIOMARIN PHARMACEUTICAL INC

    Sponsor: BIOMARIN PHARM. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 20, 2025approval282d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: AMNEAL PHARMS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 20, 2025approval282d agoPOTASSIUM CHLORIDE — FDA approvalPOTASSIUM CHLORIDE

    Sponsor: AUROBINDO PHARMA. Form: SOLUTION. Route: ORAL

    full page →POTASSIUM CHLORIDE →fda approvals ↗
    ›Nov 20, 2025approval282d agoIMULDOSA (USTEKINUMAB-SRLF) — FDA approvalustekinumab biosimilar

    Sponsor: ACCORD BIOPHARMA INC.. Form: INJECTABLE. Route: INTRAVENOUS

    full page →ustekinumab biosimilar →fda approvals ↗
    ›Nov 20, 2025approval282d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

    Sponsor: ELI LILLY AND CO. Form: CAPSULE. Route: ORAL

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval282d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

    Sponsor: ELI LILLY AND CO. Form: CAPSULE. Route: ORAL

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval282d agoSERTRALINE HYDROCHLORIDE — FDA approvalSERTRALINE HYDROCHLORIDE

    Sponsor: AUROBINDO PHARMA. Form: TABLET. Route: ORAL

    full page →SERTRALINE HYDROCHLORIDE →fda approvals ↗
    ›Nov 20, 2025approval282d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

    Sponsor: ELI LILLY AND CO. Form: CAPSULE. Route: ORAL

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval282d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

    Sponsor: ELI LILLY AND CO. Form: CAPSULE. Route: ORAL

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval282d agoCLOBETASOL PROPIONATE — FDA approvalClobetasol Propionate Teva

    Sponsor: XIROMED. Form: AEROSOL, FOAM. Route: TOPICAL

    full page →Clobetasol Propionate Teva →fda approvals ↗
    ›Nov 20, 2025device 510k282d agoResponse Ortho Solutions, LLC — The Response Ortho Smart Fixator - Hexapod System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoSi Solutions, LLC — OptumSI Implant System (510k cleared)Evita Solutions LLC

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoRemington Medical, Inc. — VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoGuangzhou Heygears IMC., Inc. — UltraPrint-Dental Denture UV (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoClassys, Inc. — CuRAS hybrid (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoHardy Diagnostics — HardyDisk AST Cefiderocol 30µg (FDC30) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoRoche Molecular Systems, Inc. — cobas liat Bordetella panel nucleic acid test (510k cleared)

    Product code: OZZ. Advisory committee: Microbiology. Type: Dual Track

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoSiemens Healthineers AG — syngo.MR Applications (VB80) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoGuangzhou Potent Medical Equipment Joint-Stock Co., Ltd. — Laser Fiber (PT-OF-A-S); Laser Fiber (PT-OF-B-S); Laser Fiber (PT-OF-C-S); Laser Fiber (PT-OF-D-S); Laser Fiber (PT-OF-E-S); Laser Fiber (PT-OF-F-S) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoCosylab Jsc, Control System Laboratory — PlanOne 1 (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoShalby Advanced Technologies, Inc. Dba Consensus Orthopedics — TaperSet™ Hip System (510k cleared)

    Product code: LPH. Advisory committee: Orthopedic. Type: Special

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoProvidence Medical Technology, Inc. — CORUS-LX Implant (510k cleared)

    Product code: MRW. Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoHangzhou Kangji Medical Instrument Co., Ltd. — Disposable Polymer Ligation Clips (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoIntegrated Endoscopy, Inc. — Nuvis® Wireless HD Camera System (Nuvis-2K) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoMedline Industries, LP — Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k282d agoSiemens Shenzhen Magnetic Resonance , Ltd. — MAGNETOM Free.Max; MAGNETOM Free.Star (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device pma282d agoMedtronic, Inc. — Sphere-9 TM Mapping and Ablation Catheter (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoTiger Aesthetics Medical, LLC — Sientra Silicone Gel Breast Implants (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: FTR. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoABBOTT MEDICAL — IsoFlex™ Pacing Leads (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: NVN. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoIntegrum AB — OPRA Implant System, Abutment component (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: PJY. Advisory committee: OR. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoABBOTT MEDICAL — Quartet™ and QuickFlex™ µ Left Heart Leads (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: NIK. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoMedibeacon, Inc. — MediBeacon® Transdermal GFR Measurement System (GFR) (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoABBOTT MEDICAL — Durata™ Defibrillation Leads (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: LWS. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoABBOTT MEDICAL — Tendril™ MRI Pacing Leads / Assurity MRI, Endurity MRI, Zenex MRI, Zenus MRI Pacemakers (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: LWP. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma282d agoABBOTT MEDICAL — OptiSense™ Pacing Leads (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: NVN. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
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