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13,554 catalysts · 3,415 8k filing · 2,401 grant · 2,136 approval · 1,479 device 510k · 1,105 device recall · 1,000 device adverse event

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  • 8k filing3,415
  • grant2,401
  • approval2,136
  • device 510k1,479
  • device recall1,105
  • device adverse event1,000
device pma
977
  • earnings584
  • recall376
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 17, 2025

    50
    ›Nov 20, 2025device pma273d agoMedtronic, Inc. — Sphere-9 TM Mapping and Ablation Catheter (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoTiger Aesthetics Medical, LLC — Sientra Silicone Gel Breast Implants (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: FTR. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoABBOTT MEDICAL — IsoFlex™ Pacing Leads (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoIntegrum AB — OPRA Implant System, Abutment component (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: PJY. Advisory committee: OR. Decision: APPR

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoABBOTT MEDICAL — Quartet™ and QuickFlex™ µ Left Heart Leads (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoMedibeacon, Inc. — MediBeacon® Transdermal GFR Measurement System (GFR) (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoABBOTT MEDICAL — Durata™ Defibrillation Leads (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoABBOTT MEDICAL — Tendril™ MRI Pacing Leads / Assurity MRI, Endurity MRI, Zenex MRI, Zenus MRI Pacemakers (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 20, 2025device pma273d agoABBOTT MEDICAL — OptiSense™ Pacing Leads (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 20, 2025device recall273d agoCareFusion 303, Inc. device recall (Cls II)

    BD Pyxis MedStation ES, REF: 323, BD Pyxis MedStation ES 7 Drawer Auxiliary, REF: 324, BD Pyxis MedStation ES Tower, REF: 352, BD Pyxis Pro 7-Drawer Auxiliary, REF: 1149-00, BD Pyxis Pro 7- Drawer Auxiliary with Secure Tower, REF: 1152-00, BD Pyxis Pro MedStation Main, REF: 1155-00, BD Pyxis CII Safe ES, REF: 1116-00 — Reason: Automated Dispensing Cabinets (ADC) received a Half Height CUBIE drawer firmware update, which caused a Cubie Insert event which prompts software to generate a duplicate address, which causes an error and the drawer to fail, which may lead to inability or delay in accessing stored items, delay in the replenishment of ADCs or patient specific medications stored outside of ADCs. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 20, 2025device recall273d agoMedtronic Neuromodulation device recall (Cls II)

    Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT900A CLINICIAN TABLET US CT900B PROG CT900B CLINICIAN TABLET EU -UK CT900C PROG CT900C CLINICIAN TABLET UK CT900D PROG CT900D CLINICIAN TABLET GLOBAL CT900E PROG CT900E CLINICIAN TABLET GLBL SMSNG CT900F PROG CT900F CLINICIAN TABLET GLBL SMSNG — Reason: Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and the patient experienced a recurrence of underlying pain symptoms. Resolution would require surgical replacement of the INS. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 21, 2025approval272d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

    Sponsor: MERCK SHARP DOHME. Form: SOLUTION. Route: INTRAVENOUS

    full page →pembrolizumab →fda approvals ↗
    ›Nov 21, 2025approval272d agoKEYTRUDA QLEX (PEMBROLIZUMAB) — FDA approval(berahyaluronidase alfa + pembrolizumab)

    Sponsor: MERCK SHARP DOHME. Form: INJECTABLE. Route: INJECTION

    full page →(berahyaluronidase alfa + pembrolizumab) →fda approvals ↗
    ›Nov 21, 2025approval272d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Nov 21, 2025approval272d agoNARCAN (NALOXONE HYDROCHLORIDE) — FDA approvalEmergent Devices Inc

    Sponsor: EMERGENT. Form: SPRAY, METERED. Route: NASAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval272d agoNEXLETOL (BEMPEDOIC ACID) — FDA approvalbempedoic acid

    Sponsor: ESPERION THERAPS INC. Form: TABLET. Route: ORAL

    full page →bempedoic acid →fda approvals ↗
    ›Nov 21, 2025approval272d agoNEXLIZET (BEMPEDOIC ACID) — FDA approval(bempedoic acid + ezetimibe)

    Sponsor: ESPERION THERAPS INC. Form: TABLET. Route: ORAL

    full page →(bempedoic acid + ezetimibe) →fda approvals ↗
    ›Nov 21, 2025approval272d agoLIVTENCITY (MARIBAVIR) — FDA approvalTakeda Pharmaceuticals USA Inc

    Sponsor: TAKEDA PHARMS USA. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval272d agoURSODIOL — FDA approvalURSODIOL

    Sponsor: STRIDES PHARMA. Form: CAPSULE. Route: ORAL

    full page →URSODIOL →fda approvals ↗
    ›Nov 21, 2025approval272d agoUNLOXCYT (COSIBELIMAB-IPDL) — FDA approvalcosibelimab

    Sponsor: CHECKPOINT THERAPEUTICS INC. Form: INJECTABLE. Route: INJECTION

    full page →cosibelimab →fda approvals ↗
    ›Nov 21, 2025approval272d agoDALFAMPRIDINE — FDA approvalSolaxa Inc

    Sponsor: ALKEM LABS LTD. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval272d agoFULVESTRANT — FDA approvalFULVESTRANT

    Sponsor: AVYXA HOLDINGS. Form: SOLUTION. Route: INTRAMUSCULAR

    full page →FULVESTRANT →fda approvals ↗
    ›Nov 21, 2025approval272d agoBACLOFEN — FDA approvalBACLOFEN

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

    full page →BACLOFEN →fda approvals ↗
    ›Nov 21, 2025approval272d agoPYLERA (BISMUTH SUBCITRATE POTASSIUM) — FDA approval

    Sponsor: LABS JUVISE. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval272d agoAKTEN (LIDOCAINE HYDROCHLORIDE) — FDA approvalLaryng-O-Jet

    Sponsor: THEA PHARMA. Form: GEL. Route: OPHTHALMIC

    full page →Laryng-O-Jet →fda approvals ↗
    ›Nov 21, 2025approval272d agoDEFLAZACORT — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: UPSHER SMITH LABS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval272d agoLEVETIRACETAM — FDA approvalAprecia Pharmaceuticals LLC

    Sponsor: ANDA REPOSITORY. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Nov 21, 2025approval272d agoPADCEV (ENFORTUMAB VEDOTIN-EJFV) — FDA approvalenfortumab vedotin

    Sponsor: ASTELLAS. Form: INJECTABLE. Route: INJECTION

    full page →enfortumab vedotin →fda approvals ↗
    ›Nov 21, 2025approval272d agoDIPRIVAN (PROPOFOL) — FDA approvalPROPOFOL

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

    full page →PROPOFOL →fda approvals ↗
    ›Nov 21, 2025approval272d agoALBUTEROL SULFATE — FDA approvalALBUTEROL SULFATE

    Sponsor: CIPLA. Form: AEROSOL, METERED. Route: INHALATION

    full page →ALBUTEROL SULFATE →fda approvals ↗
    ›Nov 21, 2025approval272d agoQOLIANA (BRIMONIDINE TARTRATE) — FDA approvalLumify

    Sponsor: SANDOZ. Form: SOLUTION/DROPS. Route: OPHTHALMIC

    full page →Lumify →fda approvals ↗
    ›Nov 21, 2025device 510k272d agoEffortmed, LLC — EffortMed PEEK Cages & Corpectomy Cages (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoNGMedical GmbH — BEE HA (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoNeuro Event Labs OY — Nelli (Version 7.11) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoDeroyal Industries, Inc. — Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory (510k cleared)ABM INDUSTRIES INC /DE/

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoFoshan Kycare Medical Equipment Co., Ltd. — Oxygen Concentrator (J5A) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoGraphy, Inc. — TERA HARZ Hard Denture (THD-C-500); TERA HARZ Hard Denture (THD-C-1000); TERA HARZ Hard Denture (THD-LP-500); TERA HARZ Hard Denture (THD-LP-1000); TERA HARZ Hard Denture (THD-P-500); TERA HARZ Hard Denture (THD-P-1000); TERA HARZ Hard Denture (THD-CP-500); TERA HARZ Hard Denture (THD-CP-1000) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoCentrix, Inc. — FluoroDose Varnish (510k cleared)CentricsBio Inc

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoJoint Preservation Innovations, LLC — Articulator Arthroscopic Bur (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoEveryway Medical Instruments Co.,Ltd — Li-Battery Powered OTC TENS/EMS Combination Stimulator, Model Z4 (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoStaclear, Inc. — StaClear Syringe (SC250AN); StaClear Syringe (SC250LS); StaClear Syringe (SC250LL) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoTerumo Corporation — Pen Injector Needle 32.5 (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoPhasor Health, LLC — LEGACY (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoSuzhou Master Machinery Manufacturing Co.,Ltd — Manual Wheelchair (HM305-Air1, HM305-Air2) (510k cleared)

    Product code: IOR. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoIcardio.Ai — CardioVision (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoArchy Dental, Inc. — Archy Dental Imaging (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoIntradin (Shanghai) Machinery Co., Ltd. — Powered Mobility Scooter (PMS105, GUT177, GCAT047) (510k cleared)

    Product code: INI. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoCeribell, Inc. — Ceribell Infant Seizure Detection Software (510k cleared)Ceribell, Inc.

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device 510k272d agoDentsply Sirona — Atlantis® Abutments in Titanium for Straumann BLX and Neodent GM Implants (510k cleared)DENTSPLY SIRONA Inc.

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

    full page →fda device 510k ↗
    ›Nov 21, 2025device pma272d agoLife Technologies Corporation — Oncomine™ Dx Target Test (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: PQP. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
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    $MDT93.88+1.94%
    $CCCC
    $ESPR
    $ESPR
    $AMRX18.190.00%
    $ABM
    $XRAY11.15+0.41%
    $CBLL19.55-2.25%