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18,134 catalysts · 4,728 grant · 3,126 8k filing · 2,627 approval · 2,156 device 510k · 1,745 device recall · 1,501 device pma

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  • grant4,728
  • 8k filing3,126
  • approval2,627
  • device 510k2,156
  • device recall1,745
  • device pma1,501
  • device adverse event1,000
  • recall586
  • earnings583
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Aug 11, 2025

    50
    ›Aug 13, 2025device recall364d agoPenner Patient Care, Inc. device recall (Cls III)

    Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2 — Reason: The device does not bear a unique device identifier. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device recall364d agoPhilips North America Llc device recall (Cls II)

    Philips CT systems labeled as the following: 1. Brilliance iCT SP, Model Number: 728311. — Reason: The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 13, 2025device 510k364d agoBaisheng Medical Co., Ltd. — Electrotherapy Electrodes (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoBruker Daltonics GmbH & Co. KG — MBT Compass HT CA Software; MBT FAST Shuttle US IVD (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoE.M.S Electro Medical Systems S.A — DOLORCLAST Focused Shock Waves (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoUnibeauty (Hubei) Technology Co., Ltd. — Unscented menstrual long applicator tampon; Unscented menstrual Compact Applicator Tampon; Unscented menstrual Cardboard Applicator Tampon; Unscented menstrual Digital Tampons (510k cleared)

    Product code: HEB. Advisory committee: Obstetrics/Gynecology. Type: Special

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoPipeline Medical Products, LLC — AeroJet Ventilation Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoNuwellis, Inc. — Dual Lumen Extended Length Catheter (dELC), 6F, 12cm (320101); Dual Lumen Extended Length Catheter (dELC), 6F, 16 cm (320102) (510k cleared)Nuwellis, Inc.

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoAppliedvr — RelieVRx (Pico G3) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoKarl Storz SE & CO. KG — KARL STORZ HOPKINS Telescopes for Urology (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoUnimed Medical Supplies, Inc. — Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U403-117); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U103-117); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U410-121); Unimed Reusable SpO2 Sensors (-117 and -121 Series) (U110-121) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoOsstem Implant Co., Ltd. — Bone Screw (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoS.I.N. Implant System Ltda — S.I.N. Dental Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoHuizhou Lvb Maternal and Infant Supplies Co., Ltd. — Wearable Breast Pump (P9, P10, P16, P20, P21, P22, P23, P25) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoStryker GmbH — T2 Alpha Femur Retrograde Nailing System (510k cleared)STRYKER CORP

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

    full page →fda device 510k ↗
    ›Aug 13, 2025device 510k364d agoRiverpoint Medical — HS Fiber (510k cleared)

    Product code: GAT. Advisory committee: General, Plastic Surgery. Type: Special

    full page →fda device 510k ↗
    ›Aug 14, 2025approval363d agoOTULFI (USTEKINUMAB-AAUZ) — FDA approvalOTULFI

    Sponsor: FRESENIUS KABI USA. Form: INJECTABLE. Route: INJECTION

    full page →OTULFI →fda approvals ↗
    ›Aug 14, 2025approval363d agoOTULFI (USTEKINUMAB-AAUZ) — FDA approvalOTULFI

    Sponsor: FRESENIUS KABI USA. Form: INJECTABLE. Route: INJECTION

    full page →OTULFI →fda approvals ↗
    ›Aug 14, 2025approval363d agoLAZCLUZE (LAZERTINIB MESYLATE) — FDA approvallazertinib mesylate

    Sponsor: JANSSEN BIOTECH. Form: TABLET. Route: ORAL

    full page →lazertinib mesylate →fda approvals ↗
    ›Aug 14, 2025approval363d agoRYBREVANT (AMIVANTAMAB-VMJW) — FDA approvalamivantamab

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

    full page →amivantamab →fda approvals ↗
    ›Aug 14, 2025device pma363d agoBoston Scientific Corp — Blazer™ Open-Irrigated Ablation Catheter (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoMicro Therapeutics, Inc. d/b/a ev3 Neurovascular — Pipeline™ Vantage Embolization Device with Shield Technology™ (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoAllergan — Juvéderm Voluma XC, Juvéderm Vollure XC, Juvéderm Volbella XC, Juvéderm Volux XC and SKINVIVE by Juvéderm (hereafter ref (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LMH. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoBoston Scientific Corp — ROTABLATOR™ Rotational Atherectomy System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoGeneoscopy, Inc. — ColoSense® (PMA supplement)

    Supplement type: 30-Day Notice. Product code: SBB. Advisory committee: PA. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoEndotronix, Inc. — Cordella Pulmonary Artery Sensor System (CorPASS) (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoFarapulse, Inc. — FARAPULSE™ Pulsed Field Ablation System (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoBoston Scientific — Blazer™ II XP Cardiac Ablation Catheter and Cable (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoAllergan — Juvéderm Ultra XC, and Juvéderm Ultra Plus XC (hereafter referred to as Ultra XC and Ultra Plus XC) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LMH. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoSiemens Medical Solutions Diagnostics Limited — IMMULITE 2000 Systems Free Prostate-Specific Antigen (Free PSA) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTG. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoSiemens Healthcare Diagnostics, Inc. — IMMULITE 2000 Prostate-Specific Antigen (PSA) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MTF. Advisory committee: IM. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoColoplast Corp. — Titan Inflatable Penile Prosthesis (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoMedtronic, Inc. — Medtronic CoreValve™ Evolut™ PRO Transcatheter Aortic Valve; Medtronic Evolut™ PRO+ Transcatheter Aortic Valve; Medtroni (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoBoston Scientific Corp — Blazer™ II Cardiac Ablation System and Cable (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoBoston Scientific Corporation — POLARx™ Cryoablation System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoMedtronic Neuromodulation — Master Restore™, Itrel™, Synergy™, Intellis™, Vanta™ and Inceptiv™ Spinal Cord Stimulation Systems and Pisces™, Specify™ (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LGW. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Aug 14, 2025device pma363d agoIntegrum AB — OPRA™ Implant System (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 14, 2025device 510k363d agoGuangzhou Ajax Medical Equipment Co., Ltd. — Cassette Autoclave (ACA5) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoShenzhen Kaiyan Medical Equipment Co., Ltd. — TRUDERMAL Pro (ZLD-390) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoGM Dos Reis Industria e Comercio Ltda. — Stitch Cerclage – Suture Tapes (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoForus Health Pvt.Ltd — 3nethra neo HD FA; 3nethra neo HD (510k cleared)

    Product code: HKI. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoMom Incubators Limited — mOm Essential Incubator (ME1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoStryker Sustainability Solutions — Reprocessed HARMONIC 700 Shears (HAR723/Reprocessed HARMONIC 700, 5mm Diameter Shears with Advanced Hemostasis x 23cm); Reprocessed HARMONIC 700 Shears (HAR736/Reprocessed HARMONIC 700, 5mm Diameter Shears with Advanced Hemostasis x 36cm); Reprocessed HARMONIC 700 Shears (HAR745/Reprocessed HARMONIC 700, 5mm Diameter SHears with Advanced Hemostasis x 45cm) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoShenzhen Leaflife Technology Co., Ltd. — WinForth (LM-E470KA) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoMaine Molecular Quality Controls, Inc. — FilmArray GI Control Panel M238 (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoBiofire Diagnostics, LLC — BIOFIRE SPOTFIRE Respiratory/Sore Throat Panel Mini (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoGeistlich Pharma AG — Geistlich Bio-Gide; Geistlich Bio-Gide® Shape; Geistlich Bio-Gide® Compressed; Geistlich Bio-Gide® Forte; Geistlich Bio-Gide® Perio; Geistlich Combi-Kit Collagen®; Geistlich Perio-System Combi Pack (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 14, 2025device 510k363d agoShenzhen Mlay Intelligent Technology Co., , Ltd. — IPL Hair Removal Device (Model(s): T14B, T16B, T19B, T15B, T17C, T18B, T21A, T21B, T21C, T21D, T22A, T22B, T25B, T25C) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 15, 2025approval362d agoBYOOVIZ (RANIBIZUMAB-NUNA) — FDA approvalBYOOVIZ

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: INJECTABLE. Route: INJECTION

    full page →BYOOVIZ →fda approvals ↗
    ›Aug 15, 2025approval362d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
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