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12,103 catalysts · 3,603 8k filing · 2,280 grant · 1,746 approval · 1,120 device 510k · 1,000 device adverse event · 821 device pma

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  • 8k filing3,603
  • grant2,280
  • approval1,746
  • device 510k1,120
  • device adverse event1,000
  • device pma821
  • device recall602
  • earnings585
  • recall266
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Dec 15, 2025

    50
    ›Dec 17, 2025device pma255d agoMentor Worldwide, LLC — MENTOR™ MemoryShape™ Breast Implants (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoInspire Medical Systems — INSPIRE II UPPER AIRWAY STIMULATOR (PMA supplement)Inspire Medical Systems, Inc.

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoEdwards Lifesciences, LLC — Edwards INSPIRIS RESILIA Aortic Valve, Model 11500A, Sizes 19mm, 21mm, 23mm, 25mm, 27mm, and 29mm; Edwards KONECT RESILI (PMA supplement)Edwards Lifesciences Corp

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoBiotronik, Inc. — Astron (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoMentor Corp. — MENTOR™ MemoryGel™ Silicone Gel-Filled Breast Implants (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoBoston Scientific Corp — Vercise Deep Brain Stimulation (DBS) Systems (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoHologic, Inc. — NovaSure Model 10 RF Controller (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MNB. Advisory committee: OB. Decision: OK30

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoMedtronic, Inc. — Activa™ Deep Brain Stimulation Therapy System (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoSyncardia Systems, LLC — SynCardia Total Artificial Heart (STAH) system (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoKeri Medical SA — TOUCH® CMC 1 Prosthesis (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoCorcym S.r.l. — Carbomedics Prosthetic Heart Valve; Carbomedics® Supra-annular Prosthetic Heart Valve; Carbo-Seal® Ascending Aortic Pros (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoLivaNova USA, Inc. — VNS THERAPY SYSTEM (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoCooperVision, Inc. — MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoInstylla, Inc. — Embrace™ Hydrogel Embolic System (HES) (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoABBOTT MEDICAL — HeartMate II™ Left Ventricular Assist System (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoBoston Scientific Corp — ALTRUA™ 2 (Model S722); ESSENTIO™ (Model L121); PROPONENT™ (Model L221); ACCOLADE™ (Model L321) (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoIntegra LifeSciences Corporation — DuraSeal Dural Sealant System (PMA supplement)INTEGRA LIFESCIENCES HOLDINGS CORP

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoBiotronik, Inc. — Astron Pulsar; Pulsar-18; Pulsar-18 T3 (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d 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 ↗
    ›Dec 17, 2025device pma255d agoEdwards Lifesciences, LLC — Edwards SAPIEN 3 Ultra RESILIA Transcatheter Heart Valve, Models 9755RSL20, 9755RSL23, 9755RSL26, and 9755RSL29 (PMA supplement)Edwards Lifesciences Corp

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoBoston Scientific — ESSENTIO MRI (Model L131); PROPONENT MRI (Model L231); ACCOLADE MRI (Model L331) (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoGuidant Corp. — VALITUDE™ (Model U125); VALITUDE X4 (Model U128); VISIONIST™ (Models U225, U226); VISIONIST X4 (Model U228) (PMA supplement)Guident Corp.

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoEdwards Lifesciences, LLC — Edwards SAPIEN 3 Ultra Transcatheter Heart Valve (sizes 20mm, 23mm, 26mm) 9750TFX; Edwards SAPIEN 3 Ultra RESILIA Transc (PMA supplement)Edwards Lifesciences Corp

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

    full page →fda device pma ↗
    ›Dec 17, 2025device pma255d agoMotiva USA, LLC — Motiva SmoothSilk®Round; Round Ergonomix® Silicone Gel-Filled Breast Implants (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    AlternatiV+ Screw-In Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    Genesis Push-In Suture Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    Fixone Biocomposite Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    Fixone Hybrid Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    Genesis Knotless Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    AlternatiV+ Max Knotless Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    Genesis Dual Thread Screw-In Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025device recall255d agoAju Pharm Co., Ltd. device recall (Cls II)ST Pharm Co Ltd

    Genesis Screw-In Anchor — Reason: Reports of device failure, including anchor breakage, anchor bending, anchor pull out, suture breakage, and secondary packaging breakage. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 17, 2025grant255d agoCREIGHTON UNIVERSITY — Peripheral auditory signaling regulates the cochlear efferent system

    GM grant. $291,000. PI: Hui Hong

    full page →nih reporter ↗
    ›Dec 18, 2025approval254d agoCLOMIPHENE CITRATE — FDA approvalCLOMIPHENE CITRATE

    Sponsor: COSETTE. Form: TABLET. Route: ORAL

    full page →CLOMIPHENE CITRATE →fda approvals ↗
    ›Dec 18, 2025approval254d agoVRAYLAR (CARIPRAZINE HYDROCHLORIDE) — FDA approvalCARIPRAZINE HYDROCHLORIDE

    Sponsor: ABBVIE. Form: CAPSULE. Route: ORAL

    full page →CARIPRAZINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 18, 2025approval254d agoVRAYLAR (CARIPRAZINE HYDROCHLORIDE) — FDA approvalCARIPRAZINE HYDROCHLORIDE

    Sponsor: ABBVIE. Form: CAPSULE. Route: ORAL

    full page →CARIPRAZINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 18, 2025approval254d agoVRAYLAR (CARIPRAZINE HYDROCHLORIDE) — FDA approvalCARIPRAZINE HYDROCHLORIDE

    Sponsor: ABBVIE. Form: CAPSULE. Route: ORAL

    full page →CARIPRAZINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 18, 2025approval254d agoVRAYLAR (CARIPRAZINE HYDROCHLORIDE) — FDA approvalCARIPRAZINE HYDROCHLORIDE

    Sponsor: ABBVIE. Form: CAPSULE. Route: ORAL

    full page →CARIPRAZINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 18, 2025approval254d agoNITROGLYCERIN — FDA approvalNITROGLYCERIN

    Sponsor: SOLARIS PHARMA CORP. Form: OINTMENT. Route: INTRA-ANAL

    full page →NITROGLYCERIN →fda approvals ↗
    ›Dec 18, 2025approval254d agoBUPRENORPHINE HYDROCHLORIDE — FDA approvalBUPRENORPHINE HYDROCHLORIDE

    Sponsor: ASCENT PHARMS INC. Form: TABLET. Route: SUBLINGUAL

    full page →BUPRENORPHINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 18, 2025approval254d agoNICARDIPINE HYDROCHLORIDE — FDA approvalNICARDIPINE HYDROCHLORIDE

    Sponsor: CHENGDU SHUODE. Form: INJECTABLE. Route: INJECTION

    full page →NICARDIPINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 18, 2025approval254d agoNUFYMCO (RANIBIZUMAB-LEYK) — FDA approvalNUFYMCO

    Sponsor: FORMYCON AG. Form: INJECTION

    full page →NUFYMCO →fda approvals ↗
    ›Dec 18, 2025approval254d agoVARENICLINE TARTRATE — FDA approvalVARENICLINE TARTRATE

    Sponsor: LUPIN LTD. Form: TABLET. Route: ORAL

    full page →VARENICLINE TARTRATE →fda approvals ↗
    ›Dec 18, 2025approval254d agoTENOFOVIR DISOPROXIL FUMARATE — FDA approvalTENOFOVIR DISOPROXIL FUMARATE

    Sponsor: MICRO LABS. Form: TABLET. Route: ORAL

    full page →TENOFOVIR DISOPROXIL FUMARATE →fda approvals ↗
    ›Dec 18, 2025approval254d agoHALOPERIDOL — FDA approvalCreekwood Pharmaceutical Inc

    Sponsor: CREEKWOOD PHARMS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Dec 18, 2025device 510k254d agoEdwards Lifesciences — HemoSphere Alta Advanced Monitoring Platform (ALTAALL1; ALTACR1; ALTASR1) (510k cleared)Edwards Lifesciences Corp

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

    full page →fda device 510k ↗
    ›Dec 18, 2025device 510k254d agoOvesco Endoscopy AG — OTSCneo System Set (100.03n-14n, 100.27n-31n) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2025device 510k254d agoOlympus Medical Systems Corporation — Single Use Cytology Brush V (BC-V600P-3010) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2025device 510k254d agoNatec Medical , Ltd. — Amethyst HP PTA OTW 0.035 Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 18, 2025device 510k254d agoFresenius Medical Care Renal Therapies Group, LLC — FX CorAL 40; FX CorAL 50 (510k cleared)Fresenius Medical Care AG

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

    full page →fda device 510k ↗
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