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13,210 catalysts · 3,415 8k filing · 2,401 grant · 2,059 approval · 1,416 device 510k · 1,000 device adverse event · 949 device recall

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  • 8k filing3,415
  • grant2,401
  • approval2,059
  • device 510k1,416
  • device adverse event1,000
  • device recall949
device pma
941
  • earnings584
  • 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, 2025approval274d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

    Sponsor: MACLEODS PHARMS LTD. Form: TABLET. Route: ORAL

    full page →DOXYCYCLINE HYCLATE →fda approvals ↗
    ›Nov 19, 2025approval274d agoIMDELLTRA (TARLATAMAB-DLLE) — FDA approvaltarlatamab

    Sponsor: AMGEN INC. Form: INJECTABLE. Route: INJECTION

    full page →tarlatamab →fda approvals ↗
    ›Nov 19, 2025approval274d agoNILOTINIB HYDROCHLORIDE — FDA approvalHetero Labs Ltd

    Sponsor: DR REDDYS. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 19, 2025approval274d agoHEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER (HEPARIN SODIUM) — FDA approvalHEPARIN SODIUM

    Sponsor: HOSPIRA. Form: INJECTABLE. Route: INJECTION

    full page →HEPARIN SODIUM →fda approvals ↗
    ›Nov 19, 2025approval274d agoIGALMI (DEXMEDETOMIDINE HYDROCHLORIDE) — FDA approvaldexmedetomidine

    Sponsor: BIOXCEL. Form: FILM. Route: BUCCAL, SUBLINGUAL

    full page →dexmedetomidine →fda approvals ↗
    ›Nov 19, 2025approval274d agoNILOTINIB HYDROCHLORIDE — FDA approvalNILOTINIB HYDROCHLORIDE

    Sponsor: MSN. Form: CAPSULE. Route: ORAL

    full page →NILOTINIB HYDROCHLORIDE →fda approvals ↗
    ›Nov 19, 2025approval274d agoKOSELUGO (SELUMETINIB SULFATE) — FDA approvalselumetinib sulfate

    Sponsor: ASTRAZENECA. Form: CAPSULE. Route: ORAL

    full page →selumetinib sulfate →fda approvals ↗
    ›Nov 19, 2025approval274d agoKOSELUGO (SELUMETINIB) — FDA approvalselumetinib sulfate

    Sponsor: ASTRAZENECA. Form: CAPSULE. Route: ORAL

    full page →selumetinib sulfate →fda approvals ↗
    ›Nov 19, 2025approval274d agoHYRNUO (SEVABERTINIB) — FDA approvalsevabertinib

    Sponsor: BAYER HEALTHCARE. Form: TABLET. Route: ORAL

    full page →sevabertinib →fda approvals ↗
    ›Nov 19, 2025approval274d agoROPINIROLE HYDROCHLORIDE — FDA approvalropinirole hydrochloride ER

    Sponsor: ALEMBIC. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →ropinirole hydrochloride ER →fda approvals ↗
    ›Nov 19, 2025device 510k274d agoCytovale, Inc. — IntelliSep Test (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k274d agoMedacta International S.A. — MyPAO SA guides (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k274d agoFisher & Paykel Healthcare, Ltd. — OptiPAP Junior Flexi Tube US (OPTIPAPFUS); OptiPAP Junior Nasal Prongs XXS (OPTIPAPPXXS); OptiPAP Junior Nasal Prongs XS (OPTIPAPPXS); OptiPAP Junior Nasal Prongs S (OPTIPAPPS); OptiPAP Junior Nasal Prongs M (OPTIPAPPM); OptiPAP Junior Nasal Prongs L (OPTIPAPPL); OptiPAP Junior Nasal Prongs XL (OPTIPAPPXL); OptiPAP Junior Nasal Mask XXS (OPTIPAPMXXS); OptiPAP Junior Nasal Mask XS (OPTIPAPMXS); OptiPAP Junior Nasal Mask S (OPTIPAPMS); OptiPAP Junior Nasal Mask M (OPTIPAPMM); OptiPAP Jun (510k cleared)

    Product code: SGR. Advisory committee: Anesthesiology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k274d agoDepuy Ireland UC — ATTUNE™ Total Knee System; ATTUNE™ Revision Sleeve LPS™ Femoral Adaptors (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k274d agoFusion Innovations, LLC — SternaFuse Ti Fixation System (510k cleared)Fundrise Innovation Fund, LLC

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k274d 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 510k274d agoEdap Technomed, Inc. — Focal One® (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k274d 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 510k274d 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 510k274d 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 510k274d 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 pma274d 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 pma274d 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 pma274d 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 pma274d 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 pma274d 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 recall274d 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 recall274d 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 recall274d 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, 2025grant274d 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, 2025approval273d agoPALYNZIQ (PEGVALIASE-PQPZ) — FDA approvalBIOMARIN PHARMACEUTICAL INC

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

    full page →fda approvals ↗
    ›Nov 20, 2025approval273d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalAmneal Pharmaceuticals, Inc.

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

    full page →fda approvals ↗
    ›Nov 20, 2025approval273d agoPOTASSIUM CHLORIDE — FDA approvalPOTASSIUM CHLORIDE

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

    full page →POTASSIUM CHLORIDE →fda approvals ↗
    ›Nov 20, 2025approval273d agoIMULDOSA (USTEKINUMAB-SRLF) — FDA approvalustekinumab biosimilar

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

    full page →ustekinumab biosimilar →fda approvals ↗
    ›Nov 20, 2025approval273d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval273d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval273d agoSERTRALINE HYDROCHLORIDE — FDA approvalSERTRALINE HYDROCHLORIDE

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

    full page →SERTRALINE HYDROCHLORIDE →fda approvals ↗
    ›Nov 20, 2025approval273d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval273d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval273d agoCLOBETASOL PROPIONATE — FDA approvalClobetasol Propionate Teva

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

    full page →Clobetasol Propionate Teva →fda approvals ↗
    ›Nov 20, 2025device 510k273d 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 510k273d 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 510k273d 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 510k273d 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 510k273d agoClassys, Inc. — CuRAS hybrid (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k273d 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 510k273d 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 510k273d 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 510k273d 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 510k273d agoCosylab Jsc, Control System Laboratory — PlanOne 1 (510k cleared)

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

    full page →fda device 510k ↗
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