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12,957 catalysts · 3,404 8k filing · 2,377 grant · 2,035 approval · 1,373 device 510k · 1,000 device adverse event · 929 device pma

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  • 8k filing3,404
  • grant2,377
  • approval2,035
  • device 510k1,373
  • device adverse event1,000
  • device pma929
device recall
810
  • 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 18, 2025device recall274d agoAGFA Healthcare Corp. device recall (Cls II)TENET HEALTHCARE CORP

    Brand name: AGFA Digital Radiography X- Ray system DR 800 with MUSICA Dynamic Common Name: DR 800 — Reason: It is possible to exceed the maximum allowed Air Kerma rate (AKR) of 88mGy/min for pulsed fluoro exams. This can happen in case the framerate is increased on the NX workstation when ABS is not enabled. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 18, 2025device recall274d agoDICOM Grid, Inc. device recall (Cls II)

    Intelerad InteleShare software, with ProViewer component — Reason: Software intended to aid in diagnosing conditions, planning treatments, visualizing anatomical structures has a bug that, if all of following are met: Viewing images in InteleShare viewer; Multiplanar reconstruction applied; Manual rotation applied, could result in inaccurate length measurement tool values that could compromise diagnostic accuracy, lead to misdiagnosis or inappropriate follow-up. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 18, 2025grant274d agoCASE WESTERN RESERVE UNIVERSITY — Olfactory Phenotypes as Non-Invasive Biomarkers for Alzheimer's Disease: A Ma...Case Western Reserve University

    AG grant. $746,114. PI: Jennifer Villwock

    full page →nih reporter ↗
    ›Nov 19, 2025approval273d agoEYLEA HD (AFLIBERCEPT) — FDA approvalEYLEA HD

    Sponsor: REGENERON PHARMACEUTICALS. Form: INJECTABLE. Route: INJECTION

    full page →EYLEA HD →fda approvals ↗
    ›Nov 19, 2025approval273d agoDARZALEX FASPRO (DARATUMUMAB AND HYALURONIDASE-FIHJ) — FDA approval(daratumumab + hyaluronidase (human recombinant))

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →(daratumumab + hyaluronidase (human recombinant)) →fda approvals ↗
    ›Nov 19, 2025approval273d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

    Sponsor: HIBROW HLTHCARE. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 19, 2025approval273d agoSELARSDI (USTEKINUMAB-AEKN) — FDA approvalAlvotech

    Sponsor: ALVOTECH USA INC. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 19, 2025approval273d agoNILOTINIB HYDROCHLORIDE — FDA approvalNILOTINIB HYDROCHLORIDE

    Sponsor: HETERO LABS LTD V. Form: CAPSULE. Route: ORAL

    full page →NILOTINIB HYDROCHLORIDE →fda approvals ↗
    ›Nov 19, 2025approval273d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

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

    full page →DOXYCYCLINE HYCLATE →fda approvals ↗
    ›Nov 19, 2025approval273d agoIMDELLTRA (TARLATAMAB-DLLE) — FDA approvaltarlatamab

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

    full page →tarlatamab →fda approvals ↗
    ›Nov 19, 2025approval273d agoNILOTINIB HYDROCHLORIDE — FDA approvalHetero Labs Ltd

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

    full page →fda approvals ↗
    ›Nov 19, 2025approval273d 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, 2025approval273d agoIGALMI (DEXMEDETOMIDINE HYDROCHLORIDE) — FDA approvaldexmedetomidine

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

    full page →dexmedetomidine →fda approvals ↗
    ›Nov 19, 2025approval273d agoNILOTINIB HYDROCHLORIDE — FDA approvalNILOTINIB HYDROCHLORIDE

    Sponsor: MSN. Form: CAPSULE. Route: ORAL

    full page →NILOTINIB HYDROCHLORIDE →fda approvals ↗
    ›Nov 19, 2025approval273d agoKOSELUGO (SELUMETINIB SULFATE) — FDA approvalselumetinib sulfate

    Sponsor: ASTRAZENECA. Form: CAPSULE. Route: ORAL

    full page →selumetinib sulfate →fda approvals ↗
    ›Nov 19, 2025approval273d agoKOSELUGO (SELUMETINIB) — FDA approvalselumetinib sulfate

    Sponsor: ASTRAZENECA. Form: CAPSULE. Route: ORAL

    full page →selumetinib sulfate →fda approvals ↗
    ›Nov 19, 2025approval273d agoHYRNUO (SEVABERTINIB) — FDA approvalsevabertinib

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

    full page →sevabertinib →fda approvals ↗
    ›Nov 19, 2025approval273d agoROPINIROLE HYDROCHLORIDE — FDA approvalropinirole hydrochloride ER

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

    full page →ropinirole hydrochloride ER →fda approvals ↗
    ›Nov 19, 2025device 510k273d agoCytovale, Inc. — IntelliSep Test (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k273d 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 510k273d 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 510k273d 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 510k273d 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 510k273d 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 510k273d agoEdap Technomed, Inc. — Focal One® (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 19, 2025device 510k273d 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 510k273d 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 510k273d 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 510k273d 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 pma273d 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 pma273d 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 pma273d 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 pma273d 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 pma273d 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 recall273d 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 recall273d 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 recall273d 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, 2025grant273d 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, 2025approval272d agoPALYNZIQ (PEGVALIASE-PQPZ) — FDA approvalBIOMARIN PHARMACEUTICAL INC

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

    full page →fda approvals ↗
    ›Nov 20, 2025approval272d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalAmneal Pharmaceuticals, Inc.

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

    full page →fda approvals ↗
    ›Nov 20, 2025approval272d agoPOTASSIUM CHLORIDE — FDA approvalPOTASSIUM CHLORIDE

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

    full page →POTASSIUM CHLORIDE →fda approvals ↗
    ›Nov 20, 2025approval272d agoIMULDOSA (USTEKINUMAB-SRLF) — FDA approvalustekinumab biosimilar

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

    full page →ustekinumab biosimilar →fda approvals ↗
    ›Nov 20, 2025approval272d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval272d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval272d agoSERTRALINE HYDROCHLORIDE — FDA approvalSERTRALINE HYDROCHLORIDE

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

    full page →SERTRALINE HYDROCHLORIDE →fda approvals ↗
    ›Nov 20, 2025approval272d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval272d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval272d agoCLOBETASOL PROPIONATE — FDA approvalClobetasol Propionate Teva

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

    full page →Clobetasol Propionate Teva →fda approvals ↗
    ›Nov 20, 2025device 510k272d 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 510k272d agoSi Solutions, LLC — OptumSI Implant System (510k cleared)Evita Solutions LLC

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

    full page →fda device 510k ↗
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