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13,680 catalysts · 3,369 8k filing · 2,401 grant · 2,188 approval · 1,517 device 510k · 1,123 device recall · 1,026 device pma

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  • 8k filing3,369
  • grant2,401
  • approval2,188
  • device 510k1,517
  • device recall1,123
  • device pma1,026
device adverse event
1,000
  • earnings584
  • recall391
  • 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, 2025approval271d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval271d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval271d agoSERTRALINE HYDROCHLORIDE — FDA approvalSERTRALINE HYDROCHLORIDE

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

    full page →SERTRALINE HYDROCHLORIDE →fda approvals ↗
    ›Nov 20, 2025approval271d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval271d agoRETEVMO (SELPERCATINIB) — FDA approvalselpercatinib

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

    full page →selpercatinib →fda approvals ↗
    ›Nov 20, 2025approval271d agoCLOBETASOL PROPIONATE — FDA approvalClobetasol Propionate Teva

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

    full page →Clobetasol Propionate Teva →fda approvals ↗
    ›Nov 20, 2025device 510k271d 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 510k271d agoSi Solutions, LLC — OptumSI Implant System (510k cleared)Evita Solutions LLC

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoRemington Medical, Inc. — VascuChek Kit, VascuChek Transceiver, VascuChek Clinical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-CP-01, VC-SD-01); VascuChek Kit, VascuChek Transceiver, VascuChek Surgical Probe, VascuChek Speaker Dock (VC-KIT-02, VC-TRX-02, VC-SP-01, VC-SD-01) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoGuangzhou Heygears IMC., Inc. — UltraPrint-Dental Denture UV (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoClassys, Inc. — CuRAS hybrid (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoHardy Diagnostics — HardyDisk AST Cefiderocol 30µg (FDC30) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoRoche Molecular Systems, Inc. — cobas liat Bordetella panel nucleic acid test (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoSiemens Healthineers AG — syngo.MR Applications (VB80) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoGuangzhou Potent Medical Equipment Joint-Stock Co., Ltd. — Laser Fiber (PT-OF-A-S); Laser Fiber (PT-OF-B-S); Laser Fiber (PT-OF-C-S); Laser Fiber (PT-OF-D-S); Laser Fiber (PT-OF-E-S); Laser Fiber (PT-OF-F-S) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoCosylab Jsc, Control System Laboratory — PlanOne 1 (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoShalby Advanced Technologies, Inc. Dba Consensus Orthopedics — TaperSet™ Hip System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoProvidence Medical Technology, Inc. — CORUS-LX Implant (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoHangzhou Kangji Medical Instrument Co., Ltd. — Disposable Polymer Ligation Clips (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoIntegrated Endoscopy, Inc. — Nuvis® Wireless HD Camera System (Nuvis-2K) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoMedline Industries, LP — Namic Radial Arm Band, 23 cm (DYNJRADBAND); Namic Radial Arm Band, 26 cm (DYNJRADBANDL) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device 510k271d agoSiemens Shenzhen Magnetic Resonance , Ltd. — MAGNETOM Free.Max; MAGNETOM Free.Star (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 20, 2025device pma271d 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 pma271d 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 pma271d 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 pma271d 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 pma271d 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 pma271d 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 pma271d 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 pma271d 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 pma271d 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 recall271d 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 recall271d 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, 2025approval270d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

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

    full page →pembrolizumab →fda approvals ↗
    ›Nov 21, 2025approval270d 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, 2025approval270d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Nov 21, 2025approval270d agoNARCAN (NALOXONE HYDROCHLORIDE) — FDA approvalEmergent Devices Inc

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

    full page →fda approvals ↗
    ›Nov 21, 2025approval270d agoNEXLETOL (BEMPEDOIC ACID) — FDA approvalbempedoic acid

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

    full page →bempedoic acid →fda approvals ↗
    ›Nov 21, 2025approval270d 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, 2025approval270d agoLIVTENCITY (MARIBAVIR) — FDA approvalTakeda Pharmaceuticals USA Inc

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

    full page →fda approvals ↗
    ›Nov 21, 2025approval270d agoURSODIOL — FDA approvalURSODIOL

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

    full page →URSODIOL →fda approvals ↗
    ›Nov 21, 2025approval270d agoUNLOXCYT (COSIBELIMAB-IPDL) — FDA approvalcosibelimab

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

    full page →cosibelimab →fda approvals ↗
    ›Nov 21, 2025approval270d agoDALFAMPRIDINE — FDA approvalSolaxa Inc

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

    full page →fda approvals ↗
    ›Nov 21, 2025approval270d agoFULVESTRANT — FDA approvalFULVESTRANT

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

    full page →FULVESTRANT →fda approvals ↗
    ›Nov 21, 2025approval270d agoBACLOFEN — FDA approvalBACLOFEN

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

    full page →BACLOFEN →fda approvals ↗
    ›Nov 21, 2025approval270d agoPYLERA (BISMUTH SUBCITRATE POTASSIUM) — FDA approval

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

    full page →fda approvals ↗
    ›Nov 21, 2025approval270d agoAKTEN (LIDOCAINE HYDROCHLORIDE) — FDA approvalLaryng-O-Jet

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

    full page →Laryng-O-Jet →fda approvals ↗
    ›Nov 21, 2025approval270d agoDEFLAZACORT — FDA approvalAmneal Pharmaceuticals, Inc.

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

    full page →fda approvals ↗
    ›Nov 21, 2025approval270d agoLEVETIRACETAM — FDA approvalAprecia Pharmaceuticals LLC

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

    full page →fda approvals ↗
    ›Nov 21, 2025approval270d agoPADCEV (ENFORTUMAB VEDOTIN-EJFV) — FDA approvalenfortumab vedotin

    Sponsor: ASTELLAS. Form: INJECTABLE. Route: INJECTION

    full page →enfortumab vedotin →fda approvals ↗
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    $ESPR
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