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12,031 catalysts · 3,350 8k filing · 2,283 grant · 1,778 approval · 1,169 device 510k · 1,000 device adverse event · 849 device pma

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  • 8k filing3,350
  • grant2,283
  • approval1,778
  • device 510k1,169
  • device adverse event1,000
  • device pma849
device recall
655
  • earnings584
  • recall282
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Dec 15, 2025

    50
    ›Dec 18, 2025device pma242d agoChannel Medsystems, Inc. — Cerene® Cryotherapy Device (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: MNB. Advisory committee: OB. Decision: APPR

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoZOLL Medical Corporation — X Series®; Propaq MD®; AED 3™ BLS; Zenix Professional Defibrillators (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoMedtronic Minimed, Inc. — MiniMed 670G System (PMA supplement)Medtronic USA Inc

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoBiotronik, Inc. — Solia S 53 377177; Solia S 60 377179 (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoMedtronic, Inc. — Activa Deep Brain Stimulation Therapy System, Percept PC; BrainSense (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoZOLL Medical Corporation — AED 3™ (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoIntrinsic Therapeutics — Barricaid® Annular Closure Device (PMA supplement)Insignis Therapeutics Inc

    Supplement type: 30-Day Notice. Product code: QES. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoBaxter Bio Science — Coseal Applicator Tips (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoNeomend, Inc. — PROGEL™ Pleural Air Leak Sealant (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NBE. Advisory committee: AN. Decision: OK30

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoMedtronic Neuromodulation — Master Restore, Itrel, Synergy Intellis, Vanta and Inceptiv Spinal Cord Stimulation Systems and Pisces, Specify, and Vec (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoSymatese — Evolysse® FORM (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoBoston Scientific Corp — WaveWriter Alpha Spinal Cord Stimulator (SCS) Mixed Systems, M8 Adaptor (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoBiotronik, Inc. — Acticor Sky VR-T 481989, Rivacor Sky VR-T 481984, Rivacor Rise VR-T 482020, Rivacor Aura VR-T 482015, Acticor Sky VR-T D (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoOcclutech Holding AG — Occlutech ASD Occluder; Occlutech Pistol Pusher (OPP); Occlutech ASD Occluder Procedure Pack (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoSpectranetics (Philips) — GlideLight Laser Sheath (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoDepuy, Inc. — ATTUNE™ Revision Rotating Platform (RP) Knee System (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: NJL. Advisory committee: OR. Decision: APPR

    full page →fda device pma ↗
    ›Dec 18, 2025device pma242d agoVasorum, Ltd. — CELT ACD Vascular Closure Device (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 18, 2025device recall242d agoWilson-Cook Medical Inc. device recall (Cls II)PATH

    Teslatome Bipolar Sphincterotomes REF: TESLA-B2535-260 Model Number: G60784 UDI-DI code: 00827002607842 REF: TESLA-B2535-450 Model Number: G60785 UDI-DI code: 00827002607859 These devices are used for cannulation of the ductal system and for sphincterotomy. If preloaded, the device also aids in bridging difficult strictures during ERCP. It is indicated for sphincterotome-aided, wire-guided selective cannulation of the biliary ducts. — Reason: Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 18, 2025device recall242d agoCommunity Products, LLC device recall (Cls II)

    Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. — Reason: Potential for fraying on the body support strap. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 18, 2025device recall242d agoCommunity Products, LLC device recall (Cls II)

    Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion. — Reason: Potential for fraying on the body support strap. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 18, 2025device recall242d agoVascutek, Ltd. device recall (Cls II)

    Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE, 631516PE, 636016PE, 631220PE, 631608PE, 631206PE, 631407P50E, 631508PE, 636008PE, 636006PE, 632518PE, 634008PE, 634006PE, 631218PE, 632211PE, 634007PE, 633006PE, 631506PE, 632524PE, 636007PE, 631512PE, 636012PE, 636014PE, 632211P50E, 633016PE, 631407PE, 631809PE, 632010PE, 631608P50E, 632520PE, 632412PE, 631510PE, 635022PE, 631224PE, 632412P50E, 631507PE, 633014PE, 632010P50E, 635020PE, 631809P50E. Gelweave, REF: 736038E, 736036E, 736034E, 736032ST/10DE, 736032E, 736030ST/10DE, 736030E, 736028ST/10DE, 736028E, 736026ST/10DE, 736026E, 736024ST/10DE, 736024E, 736022ST/10DE, 736022E, 736020E, 736018E, 736016E, 736014E, 736012E, 736010E, 736008E, 736006E, 735034ST/8AE, 735034/8RME, 735034/10SEE, 735034/10RME, 735032STE, 735032ST/8AE, 735032/8SE, 735032/8RME, 735032/10SEE, 735032/10RME, 735030STE, 735030ST/8AE, 735030/8SE, 735030/8RME, 735030/10SEE, 735030/10RME, 735028STE, 735028ST/8AE, 735028E, 735028/8SE, 735028/8RME, 735028/10RME, 735026STE, 735026ST/8AE, 735026E, 735026/8SE, 735026/8RME, 735026/10RME, 735024STE, 735024ST/8AE, 735024E, 735024/8SE, 735024/8RME, 735024/10SEE, 735024/10RME, 735022STE, 735022E, 735022/8SE, 735022/8RME, 735020E, 735020/8RME, 735018E, 734038E, 734036E, 734034E, 734034CX4RMSE, 734034/8E, 734034/10E, 734032E, 734032CX4RMSE, 734032/8E, 734032/10E, 734030E, 734030CX4RMSE, 734030/8E, 734030/10E, 734028CX4RMSE, 734028/8E, 734028/10E, 734026CX4RMSE, 734026/8E, 734026/10E, 734024CX4RMSE, 734024/8E, 734024/10E, 734022CX4RMSE, 734022/8E, 734022/10E, 734020CX4RMSE, 734020/8E, 734020/10E, 734018/8E, 73341088E, 73341088/8RME, 73341088/8E, 73341088/10RME, 73341088/10E, 73321488/8ARME, 7332148/10RMFE, 7332148/10RMEE, 733212810/10STDE, 7332128/10RMFE, 7332128/10RMEE, 73321088E, 73321088/8SDE, 73321088/8RME, 73321088/8E, 73321088/10RME, 73321088/10E, 7330888/8E, 7330668/6E, 733038E, 733036E, 733034E, 733032E, 733030E, 733028E, 733026E, 733024E, 733024/6AE, 733022E, 733022/6AE, 733020E, 733020/6AE, 733018E, 733018/6AE, 733016E, 733014E, 73301488/8ARME, 7330148/10RMFE, 7330148/10RMEE, 73301412/10ETE, 733012E, 733012810/10STDE, 7330128/10RMFE, 7330128/10RMEE, 733010E, 73301088E, 73301088/8SDE, 73301088/8RME, 73301088/8E, 73301088/10RME, 73301088/10E, 733010108/8S4E, 733010108/8RME, 733010/10RME, 733008E, 733006E, 7328888/8E, 7328668/6E, 73281488/8ARME, 7328148/10RMEE, 73281412/10ETE, 73281288/8E, 732812810/10STDE, 7328128/10RMFE, 7328128/10RMEE, 73281088E, 73281088/8SDE, 73281088/8RME, 73281088/8E, 73281088/10RME, 73281088/10E, 732810108/8S4E, 7326888/8E, 7326668/6E, 73261488/8ARME, 7326148/10RMEE, 732612810/10STDE, 7326128/10RMFE, 7326128/10RMEE, 73261088E, 73261088/8SDE, 73261088/8RME, 73261088/8E, 73261088/10RME, 73261088/10E, 732610108/8S4E, 732610/10RME, 732528E, 732526E, 732524E, 732522E, 732520E, 732518E, 7324888/8E, 7324668/6E, 73241488/8ARME, 7324148/10RMEE, 732412E, 732412810/10STDE, 7324128/10RMEE, 732412/6E, 73241088E, 73241088/8SDE, 73241088/8RME, 73241088/8E, 73241088/10RME, 73241088/10E, 732410108/8S4E, 73221488/8ARME, 732214/10/10CRME, 732212810/10STDE, 732212/10/8CRME, 732212/10/8ARME, 732211E, 73221088/8RME, 73221088/8E, 73221088/10E, 732210108/8S4E, 7320888/8E, 7320668/6E, 732038E, 732034E, 732034CX4RME, 732034/8E, 732034/10E, 732032E, 732032CX4RME, 732032/8E, 732032/10E, 732030E, 732030CX4RME, 732030/8E, 732030/10E, 732028CX4RME, 732028/8E, 732028/10E, 732026CX4RME, 732026/8E, 732026/10E, 732024CX4RME, 732024/8E, 732024/10E, 732022/10E, 732014/8X2E, 732014/8X2AE, 732014/10X2E, 732014/10X2AE, 732012810/10STDE, 732012/8X2E, 732012/8X2AE, 732012/10X2E, 732010E, 73201088/8RME, 73201088/8E, 732010108/8S4E, 732010/6E, 731809E, 731809/6E, 731608XL55E, 731608E, 731608/8/10RME, 731608/6E, 731608/10/10RME, 731516E, 731514E, 731512E, 731510E, 731508E, 731506E, 7314108/10RME, 731407XL55E, — Reason: Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life. Device expiry should have been calculated from gel impregnation (date of manufacture) but it was incorrectly calculated from device packaging. — Status: Ongoing

    ›Dec 18, 2025device recall242d agoCommunity Products, LLC device recall (Cls II)

    Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. The low base variant includes smaller casters and lower base frame so that the legs fit underneath beds. — Reason: Potential for fraying on the body support strap. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 18, 2025grant242d agoSTATE UNIVERSITY OF NEW YORK AT BUFFALO — Investigating the role of peripheral nerve damage in chronic Toxoplasma infec...

    AI grant. $35,157. PI: Caleb Buerger

    full page →nih reporter ↗
    ›Dec 19, 2025approval241d agoMYQORZO (AFICAMTEN) — FDA approvalaficamten

    Sponsor: CYTOKINETICS. Form: TABLET. Route: ORAL

    full page →aficamten →fda approvals ↗
    ›Dec 19, 2025approval241d agoMOUNJARO (TIRZEPATIDE) — FDA approvalZEPBOUND

    Sponsor: ELI LILLY AND CO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →ZEPBOUND →fda approvals ↗
    ›Dec 19, 2025approval241d agoDECITABINE — FDA approvalDECITABINE

    Sponsor: RELIANCE LIFE SCI. Form: INJECTABLE. Route: INTRAVENOUS

    full page →DECITABINE →fda approvals ↗
    ›Dec 19, 2025approval241d agoLUNSUMIO (MOSUNETUZUMAB-AXGB) — FDA approvalmosunetuzumab

    Sponsor: GENENTECH INC. Form: INJECTABLE. Route: INJECTION

    full page →mosunetuzumab →fda approvals ↗
    ›Dec 19, 2025approval241d agoREZDIFFRA (RESMETIROM) — FDA approvalresmetirom

    Sponsor: MADRIGAL. Form: TABLET. Route: ORAL

    full page →resmetirom →fda approvals ↗
    ›Dec 19, 2025approval241d agoREZDIFFRA (RESMETIROM) — FDA approvalresmetirom

    Sponsor: MADRIGAL. Form: TABLET. Route: ORAL

    full page →resmetirom →fda approvals ↗
    ›Dec 19, 2025approval241d agoREZDIFFRA (RESMETIROM) — FDA approvalresmetirom

    Sponsor: MADRIGAL. Form: TABLET. Route: ORAL

    full page →resmetirom →fda approvals ↗
    ›Dec 19, 2025approval241d agoJASCAYD (NERANDOMILAST) — FDA approvalnerandomilast

    Sponsor: BOEHRINGER INGELHEIM. Form: TABLET. Route: ORAL

    full page →nerandomilast →fda approvals ↗
    ›Dec 19, 2025approval241d agoBONCRESA (DENOSUMAB-MOBZ) — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: AMNEAL PHARMS LLC. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Dec 19, 2025approval241d agoOZILTUS (DENOSUMAB-MOBZ) — FDA approvalAmneal Pharmaceuticals, Inc.

    Sponsor: AMNEAL PHARMS LLC. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Dec 19, 2025approval241d agoFLONASE SENSIMIST ALLERGY RELIEF (FLUTICASONE FUROATE) — FDA approvalGlaxoSmithKline LLC

    Sponsor: HALEON US HOLDINGS. Form: SPRAY, METERED. Route: NASAL

    full page →fda approvals ↗
    ›Dec 19, 2025approval241d agoBYLVAY (ODEVIXIBAT) — FDA approvalodevixibat

    Sponsor: IPSEN. Form: CAPSULE. Route: ORAL

    full page →odevixibat →fda approvals ↗
    ›Dec 19, 2025approval241d agoACCRUFER (FERRIC MALTOL) — FDA approvalferric maltol

    Sponsor: SHIELD TX. Form: CAPSULE. Route: ORAL

    full page →ferric maltol →fda approvals ↗
    ›Dec 19, 2025approval241d agoFLONASE ALLERGY RELIEF (FLUTICASONE PROPIONATE) — FDA approvalParatek Pharmaceuticals Inc

    Sponsor: HALEON US HOLDINGS. Form: SPRAY, METERED. Route: NASAL

    full page →fda approvals ↗
    ›Dec 19, 2025approval241d agoZINGO (LIDOCAINE HYDROCHLORIDE) — FDA approvalPowder Pharmaceuticals Inc

    Sponsor: POWDER PHARMS. Form: SYSTEM. Route: INTRADERMAL

    full page →fda approvals ↗
    ›Dec 19, 2025device 510k241d agoHeartLung Corporation — AI-CVD (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoParagon 28, Inc. — Monkey Rings External Ring Fixation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoMedskin Solutions Dr. Suwelack AG — MatriDerm pluS+ Bi-Layer (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoStryker GmbH — Hoffmann LRF System (510k cleared)STRYKER CORP

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoSorin Group Italia S.R.L. — ProtekDilate Vascular Access Kit (510k cleared)

    Product code: DRE. Advisory committee: Cardiovascular. Type: Special

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoGm Dos Reis Industria E Comercio — Pectus Versa System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoCathegenix (Xiamen) Co., Ltd. — Endura™ Ureteral Stent and Stent Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoCapsoVision, Inc. — CE Deliver (DLV) (510k cleared)CapsoVision, Inc

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoOconnell Regulatory Consultants, Inc. — Vivo 45 LS (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoDiabeloop — DBLG2 (510k cleared)

    Product code: QJI. Advisory committee: Clinical Chemistry. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoSciton, Inc — JOULE 1064nm System and Accessories (510k cleared)Aston Sci Inc

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

    full page →fda device 510k ↗
    ›Dec 19, 2025device 510k241d agoMedtronic, Inc. — C320LBB Delivery System (C320LBBS45), C320LBB Delivery System (C320LBBS48), C320LBB Delivery System (C320LBBL45), C320LBB Delivery System (C320LBBL48) (510k cleared)Medtronic plc

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

    full page →fda device 510k ↗
    ← prev
    page 15 of 241
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    full page →fda device recalls ↗
    $AMRX18.15+5.10%
    $AMRX18.15+5.10%
    $MDGL507.56+0.04%
    $MDGL507.56+0.04%
    $LLY1180.16-2.25%
    $MDGL507.56+0.04%
    $CYTK74.13+0.93%
    $BSX51.83+0.27%
    $MDT91.27+0.76%
    $SYK339.21-0.55%
    $CV
    $MDT91.27+0.76%