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12,396 catalysts · 3,368 8k filing · 2,370 grant · 1,843 approval · 1,245 device 510k · 1,000 device adverse event · 880 device pma

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  • 8k filing3,368
  • grant2,370
  • approval1,843
  • device 510k1,245
  • device adverse event1,000
  • device pma880
device recall
718
  • earnings584
  • recall307
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 24, 2025

    50
    ›Nov 24, 2025device recall267d agoDraeger, Inc. device recall (Cls I)Traeger, Inc.

    Draeger Vapor 3000. Unheated, calibrated anesthetic vaporizer. — Reason: A certain component of affected devices was not delivered within specification and contained impurities. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoAbbott Diabetes Care, Inc. device recall (Cls I)TANDEM DIABETES CARE INC

    FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. — Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 24, 2025device recall267d agoAbbott Diabetes Care, Inc. device recall (Cls I)TANDEM DIABETES CARE INC

    FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System. — Reason: Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 25, 2025approval266d agoHYDROCODONE BITARTRATE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

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

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoTIZANIDINE HYDROCHLORIDE — FDA approvalZydus Therapeutics Inc

    Sponsor: ZYDUS PHARMS. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoHUMATROPE (SOMATROPIN) — FDA approvalEMD Serono Inc

    Sponsor: LILLY. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoPRED MILD (PREDNISOLONE ACETATE) — FDA approvalprednisolone acetate

    Sponsor: ABBVIE. Form: SUSPENSION/DROPS. Route: OPHTHALMIC

    full page →prednisolone acetate →fda approvals ↗
    ›Nov 25, 2025approval266d agoZEGERID OTC (OMEPRAZOLE) — FDA approvalCovis Pharmaceuticals Inc (Inactive)

    Sponsor: RILEY CONSUMER. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoENOXAPARIN SODIUM (PRESERVATIVE FREE) (ENOXAPARIN SODIUM) — FDA approvalenoxaparin sodium

    Sponsor: SHENZHEN TECHDOW. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →enoxaparin sodium →fda approvals ↗
    ›Nov 25, 2025approval266d agoIRBESARTAN — FDA approvalIRBESARTAN

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

    full page →IRBESARTAN →fda approvals ↗
    ›Nov 25, 2025approval266d agoSCEMBLIX (ASCIMINIB HYDROCHLORIDE) — FDA approvalasciminib hydrochloride

    Sponsor: NOVARTIS. Form: TABLET. Route: ORAL

    full page →asciminib hydrochloride →fda approvals ↗
    ›Nov 25, 2025approval266d agoVOYXACT (SIBEPRENLIMAB-SZSI) — FDA approvalsibeprenlimab

    Sponsor: OTSUKA PHARM CO LTD. Form: INJECTABLE. Route: INJECTION

    full page →sibeprenlimab →fda approvals ↗
    ›Nov 25, 2025approval266d agoIMFINZI (DURVALUMAB) — FDA approvalASTRAZENECA PLC

    Sponsor: ASTRAZENECA UK LTD. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoACETAZOLAMIDE — FDA approvalAccord Healthcare Inc

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

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoCHILDREN'S CETIRIZINE HYDROCHLORIDE HIVES RELIEF (CETIRIZINE HYDROCHLORIDE) — FDA approvalKenvue Inc.

    Sponsor: BAJAJ. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoPERAMPANEL — FDA approvalCATALYST PHARMACEUTICALS, INC.

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoNOREPINEPHRINE BITARTRATE — FDA approvalBaxter Healthcare Corp

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

    full page →fda approvals ↗
    ›Nov 25, 2025approval266d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

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

    full page →ALDACTAZIDE →fda approvals ↗
    ›Nov 25, 2025approval266d agoPERAMPANEL — FDA approvalPERAMPANEL

    Sponsor: MSN. Form: TABLET. Route: ORAL

    full page →PERAMPANEL →fda approvals ↗
    ›Nov 25, 2025device 510k266d agoOlympus Medical Systems Corporation — Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoIndica Labs, LLC — HALO AP Dx (510k cleared)

    Product code: QKQ. Advisory committee: Pathology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoEncore Guards — enCore Night Guard (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoStemtech Medical Devices Private Limited — Eva Scalp Cooling System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoAkura Medical — Akura Thrombectomy System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoGood Sleep CO Pte , Ltd. — Hushd Avera (510k cleared)

    Product code: LRK. Advisory committee: Dental. Type: Abbreviated

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoUzinmedicare Co., Ltd. — Spectra Platinum (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoTrustees of the University of Pennsylvania — PennPET Explorer Positron Emission Tomograph (510k cleared)University of Pennsylvania

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoShenzhen Leaflife Technology Co., Ltd. — LeafPure-Echo (LM-LPNdA) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoRay Co., Ltd. — RCT700 (510k cleared)Ray Therapeutics Inc

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoFeops NV — FEops HEARTguide Simulation Application (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoMedusa Orthopedics, LLC — Medusa Orthopedics Boa External Fixation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoDongguan Lide Electric Appliance Co., Ltd. — IPL Hair Removal Device (KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoNaox Technologies Sas — NX01 (NX01) (510k cleared)Niu Technologies

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoGeistlich Pharma AG — Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide® (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoZsfab, Inc. — ZSFab Lumbar Interbody System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoEsaote, S.p.A. — 7600 Ultrasound System (MyLabC25); 7600 Ultrasound System (MyLabC30) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoMlhealth 360 — Scaida BrainCT-ICH (v1.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoSpeclipse, Inc. — BELLUS-Q (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k266d agoLuxCreo, Inc. — LuxCreo Flexible Partial Denture Resin (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device pma266d agoMicroPort CRM USA, Inc. — ENERGYA/TALENTIA ICDs & CRT-Ds, SmartTouch Programmer Software Modules, SmartView Connect App, & RMS (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoEndotronix, Inc. — CorPASS System (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoMicroPort CRM USA, Inc. — ENERGYA/TALENTIA ICDs & CRT-Ds, SmartTouch Programmer Software Modules, SmartView Connect App, & RMS (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoLivaNova USA, Inc. — VNS Therapy Model 3100 Programmer, VNS Therapy Model 2000 Programming Wand (PMA supplement)

    Supplement type: Real-Time Process. Product code: LYJ. Advisory committee: NE. Decision: APPR

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoMicroPort CRM USA, Inc. — ENERGYA/TALENTIA ICDs & CRT-Ds, SmartTouch Programmer Software Modules, SmartView Connect App, & RMS (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoMedtronic, Inc. — Micra Transcatheter Pacing Systems (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoInstylla, Inc. — Embrace(TM) Hydrogel Embolic System (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoXvivo Perfusion, Inc. — XPS™ with Steen Solution™ Perfusate (PMA supplement)

    Supplement type: Real-Time Process. Product code: PHO. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Nov 25, 2025device pma266d agoLumicell, Inc. — Lumicell Direct Visualization System (DVS) (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: SAW. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Nov 25, 2025device recall266d agoFerndale Laboratories, Inc. device recall (Cls II)G&W Laboratories Inc

    Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 Product Description: Liquid adhesive, 2/3 mL vial, 48 vials per carton Component: No — Reason: Butyrate tube cracks during actuation, rendering product unusable. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 25, 2025grant266d agoLAUREATE INSTITUTE FOR BRAIN RESEARCH — Mechanisms of Low-Intensity Focused Ultrasound Neuromodulation for Post-Traum...

    GM grant. $431,302. PI: Adrienne A Taren

    full page →nih reporter ↗
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    $TNDM22.86+0.62%
    $KVUE19.200.00%
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    $FRTRY
    $NIU2.0800-1.42%
    $MDT91.27+0.76%