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17,754 catalysts · 4,728 grant · 3,086 8k filing · 2,606 approval · 2,051 device 510k · 1,649 device recall · 1,418 device pma

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  • grant4,728
  • 8k filing3,086
  • approval2,606
  • device 510k2,051
  • device recall1,649
  • device pma1,418
device adverse event
1,000
  • earnings583
  • recall551
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Aug 25, 2025

    50
    ›Aug 26, 2025device 510k351d agoImperative Care, Inc. — X-Wire Guidewire (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 26, 2025device 510k351d agoKitazato Corporation — Ultra-Fast Vitri; Ultra-Fast Warm (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025approval350d agoFILSPARI (SPARSENTAN) — FDA approvalsparsentan

    Sponsor: TRAVERE. Form: TABLET. Route: ORAL

    full page →sparsentan →fda approvals ↗
    ›Aug 27, 2025recall350d agoHaleon US Holdings LLC recall (Cls III)

    Sensodyne PRONAMEL (Potassium nitrate 5%, Sodium fluoride 0.25%) Active SHIELD Toothpaste for Sensitive Teeth, Fresh Mint, Net WT 3.4OZ (96.4g) Tube, 6 tubes x 2 inners, per case, Distributed by GSK Consumer Healthcare, Warren, NJ 07059. UPC 3 10158 35691 2 — Reason: Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is labelled Cool Mint/Whitening. The toothpaste inside the tube is Fresh Mint as indicated on the outer carton — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 27, 2025recall350d agoCipla USA, Inc. recall (Cls III)Cipla USA Inc

    Albuterol Sulfate, Inhalation Aerosol, 90 mcg, 200 metered Inhalations, NET CONTENT 6.7 g, Manufactured by: Cipla Ltd, Indore, SEZ, Pithampur, India; Manufactured for: Cipla USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059, NDC 69097-142-60. — Reason: Failed Stability Specifications: Out of specification results was observed in Induction Port during the analysis of Particle size distribution at the 12-month time point. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 27, 2025recall350d agoPFIZER INC recall (Cls II)PFIZER INC

    Vial Label: Epinephrine Injection, USP, 1mg/10mL (0.1 mg/mL), Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045, USA. NDC 0409-4933-05. Case: NDC 0409-4933-10. — Reason: Lack of Assurance of Sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 27, 2025recall350d agoPFIZER INC recall (Cls II)PFIZER INC

    Vial Label: 8.4% Sodium Bicarbonate Injection, USP, 50mEq/50 mL (1 mEq/mL), Rx only, Hospira, Inc., Lake Forest, IL 60045, USA, NDC 0409-6637-24. Case NDC: 00409-6637-14. — Reason: Lack of Assurance of Sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 27, 2025recall350d agoVIONA PHARMACEUTICALS INC recall (Cls II)IONIS PHARMACEUTICALS INC

    Tavaborole Topical Solution 5%, 10 mL per glass bottle, Rx Only, For Topical Use Only, Manufactured by: Zydus Lifesciences Ltd., Changodar Ahmedabad, India. Distributed by: Viona Pharmaceuticals Inc., Cranford, NJ 07016. NDC: 72578-102-04 — Reason: Discoloration — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 27, 2025recall350d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)ACI Healthcare USA Inc

    Carvedilol Tablets USP, 12.5 mg, 100- Tablets, (10x10) cartons, Rx Only, Packaged and distributed by Major Pharmaceuticals, Indianapolis, IN, 46268, USA, NDC 0904-7307-61 — Reason: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 27, 2025recall350d agoTaizhou Kangping Medical Science And Technology Co., Ltd. recall (Cls II)

    BZK Antiseptic Towelette, Sterile, For External Use Only, benzalkonium chloride 0.13%, Antiseptic, 100 towelettes per carton , For Professional use, Mfg by: Taizhou Kangping Medical, Taizhou, JiangSu, China, NDC: 71310-111-01 — Reason: Lack of Assurance of Sterility. — Status: Ongoing

    full page →fda recalls ↗
    ›Aug 27, 2025device 510k350d agoAidite (Qinhuangdao) Technology Co., Ltd. — Additively Manufactured Aligner Resin (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoDurr Dental SE — VistaSoft 4.0 and VisionX 4.0 (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoLesspine Innovations — ELID (Endoscopic Less Invasive Decompression) System (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoNanjing Yinuoji Medical Technology Co., Ltd. — Portable oxygen concentrator (W-R1(MAX)); Portable oxygen concentrator (W-R1); Portable oxygen concentrator (W-R2); Portable oxygen concentrator (W-R2(Lite)) (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoUv One Hygienics, Inc. — KnoxFog Anti-fogging Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoOxehealth Limited — Vital Signs (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoShanghai AnQing Medical Instrument Co., Ltd. — Flexible Bronchoscope (BS27U-12EU, BS27U-12US, BS38U-20EU, BS38U-20US) (510k cleared)

    Product code: EOQ. Advisory committee: Ear, Nose, Throat. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 27, 2025device pma350d agoHeartsine Technologies, Ltd. — HeartSine Technologies LLC's samaritan Public Access Automated External Defibrillators (SAM 350P, SAM 360P and SAM 450P) (PMA supplement)TAT TECHNOLOGIES LTD

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

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoKardium, Inc. — Globe® Pulsed Field System (PMA)Kardigan Inc

    Product code: QZI. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoMerz North America, Inc. — COAPTITE Injectable Implant (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: LNM. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoABBOTT MEDICAL — Avant™ DR CDDRA700Q, CDDRA700T; Gallant™ DR CDDRA500Q, CDDRA500T; Entrant™ DR CDDRA300Q, CDDRA300T; Neutrino™ NxT DR CDD (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoMedtronic, Inc. — Evolut PRO+ System, Evolut FX System, Evolut FX+ System (PMA supplement)Medtronic plc

    Supplement type: Panel Track. Product code: NPT. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoABBOTT MEDICAL — HeartMate 3™ Left Ventricular Assist System (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoHologic, Inc. — ThinPrep Processor and ThinPrep Imaging System (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoABBOTT MEDICAL — IsoFlex™ (1944) (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 27, 2025device pma350d agoABBOTT MEDICAL — Quartet™ 1456Q, 1457Q, 1458Q, 1458QL; Avant™ HF CDHFA700B, CDHFA700D, CDHFA700Q, CDHFA700T; Gallant™ HF CDHFA500B, CDHFA (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 27, 2025device recall350d agoVision RT Ltd device recall (Cls II)Rail Vision Ltd.

    The AlignRT InBore system contains six Class 1 lasers which enables the system s cameras to track the patient s position and movement. — Reason: Vision RT is informing customers of an omission identified in the Instructions for Use for AlignRT InBore systems. Information identifying the lasers and their characteristics was omitted from the Instructions for Use for the subject system as required by 21 CFR 1040,10(h), via conformance with recognized consensus standard IEC 60825-1 Ed. 3 (FDA Laser Notice 56). — Status: Ongoing

    full page →fda device recalls ↗
    ›Aug 27, 2025device 510k350d agoEdan Instruments, Inc. — Fetal & Maternal Monitor (F15A, F15A Air) (510k cleared)VEECO INSTRUMENTS INC

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoHangzhou Clongene Biotech Co., Ltd. — CLUNGENE Multi-Drug Test Easy Cup; CLUNGENE Multi-Drug Home Test Easy Cup (510k cleared)Hangzhou DAC Biotech Co Ltd

    Product code: NFT. Advisory committee: Clinical Toxicology. Type: Traditional

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoAstra Orthomed, Inc. — Phoenix Sinus Tarsi Stent System (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoBasic Medical Technology, Inc. — Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid and Xylazine in Fentanyl Citrate (510k cleared)Medical Care Technologies Inc.

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoInfection Elimination Solutions, LLC — Dermalage (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoDonnevie Medical Technology (Shanghai) Co. , Ltd. — Dewin Reproductive Media (Dewin Gamete Buffer [with HSA and without HSA]; Dewin Follicle Flushing Solution, Dewin One Step medium [with HSA and without HSA]) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoFysicon BV — QMAPP® (Hemo, Hemo Lite, PCM, GO, Hybrid) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoAtraverse Medical, Inc. — HOTWIRE RF GUIDEWIRE (901XXX); HOTWIRE RF GUIDEWIRE (902XXX) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 27, 2025device 510k350d agoQIAGEN GmbH — QIAstat-Dx Respiratory Panel Plus; QIAstat-Dx Respiratory Panel Mini (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoThermo Fisher Scientific — The Sensititre 18-24 hour MIC or Breakpoint Susceptibility System with Amikacin in the dilution range of 0.25-256 ug/mL (510k cleared)THERMO FISHER SCIENTIFIC INC.

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoChangsha Anxiang Medical Technology Co., Ltd. — OTC 4-Channel Rechargeable TENS Unit (510k cleared)

    Product code: NUH. Advisory committee: Neurology. Type: Special

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoPrior Care Science Technology, Ltd. — Medical Gas Analyzer (AG200) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoAlphatec Spine, Inc. — Proximity Anterior Cervical Plate System; Segmental Plating System (SPS) (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d ago4Dmedical Limited — CT:VQ (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoImperative Care, Inc. — Symphony™ Thrombectomy System and Symphony™ 16F 82cm Thrombectomy System (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoCompumedics Limited — Somfit D (510k cleared)

    Product code: MNR. Advisory committee: Anesthesiology. Type: Special

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoImplanet — JAZZ Spinal System (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoEizo Corporation — RadiForce GX570; RadiForce GX570-AR (510k cleared)

    Product code: PGY. Advisory committee: Radiology. Type: Abbreviated

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoBasic Medical Technology, Inc. — Powder-Free Vinyl Exam Gloves, clear (510k cleared)Medical Care Technologies Inc.

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoFH Industrie — JARVIS Glenoid Reverse Shoulder Prosthesis (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoIntuitive Surgical, Inc. — da Vinci SP Firefly Imaging System (510k cleared)INTUITIVE SURGICAL INC

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

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoSyrma Johari Medtech Limited — truFlex (510k cleared)

    Product code: NGX. Advisory committee: Physical Medicine. Type: Special

    full page →fda device 510k ↗
    ›Aug 28, 2025device 510k349d agoShenzhen Mindray Bio-Medical Electronics Co., Ltd. — SV600, SV800 Ventilator (510k cleared)

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

    full page →fda device 510k ↗
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    $IONS56.25-1.21%
    $PFE27.05+1.08%
    $PFE27.05+1.08%
    $MDT89.41+2.58%
    $TVTX60.89-0.70%
    $TATT
    $VECO59.42+2.95%
    $MDCE0.00020.00%
    $ISRG393.38+3.85%
    $TMO447.81+1.31%
    $MDCE0.00020.00%