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9,961 catalysts · 3,086 8k filing · 2,091 grant · 1,128 approval · 1,000 device adverse event · 848 device 510k · 610 device pma

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2026-08-10: 0 catalysts2026-08-11: 57 catalysts2026-08-12: 19 catalysts2026-08-13: 19 catalysts2026-08-14: 4 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 2 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 1 catalyst2026-08-27: 1 catalyst2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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  • 8k filing3,086
  • grant2,091
  • approval1,128
  • device adverse event1,000
  • device 510k848
  • device pma610
earnings
583
  • device recall318
  • recall215
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jan 5, 2026

    33
    ›Jan 9, 2026approval215d agoMETHYLPHENIDATE HYDROCHLORIDE — FDA approvalMETHYLPHENIDATE HYDROCHLORIDE

    Sponsor: ABHAI LLC. Form: SOLUTION. Route: ORAL

    full page →METHYLPHENIDATE HYDROCHLORIDE →fda approvals ↗
    ›Jan 9, 2026approval215d agoAMITRIPTYLINE HYDROCHLORIDE — FDA approvalAlgoTherapeutix SAS

    Sponsor: UNIQUE PHARM. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Jan 9, 2026approval215d agoVARENICLINE TARTRATE — FDA approvalMylan Pharmaceuticals Inc

    Sponsor: UMEDICA. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Jan 9, 2026approval215d agoEVEROLIMUS — FDA approvalEVEROLIMUS

    Sponsor: BIOCON PHARMA. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →EVEROLIMUS →fda approvals ↗
    ›Jan 9, 2026approval215d agoNEXLETOL (BEMPEDOIC ACID) — FDA approvalbempedoic acid

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

    full page →bempedoic acid →fda approvals ↗
    ›Jan 9, 2026approval215d agoNEXLIZET (BEMPEDOIC ACID) — FDA approval(bempedoic acid + ezetimibe)

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

    full page →(bempedoic acid + ezetimibe) →fda approvals ↗
    ›Jan 9, 2026approval215d agoPHYTONADIONE — FDA approvalSigyn Therapeutics, Inc.

    Sponsor: SUNNY. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Jan 9, 2026device 510k215d agoAliveCor, Inc. — Corvair Monza (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoNova Biomedical Corporation — Nova Allegro UACR Assay, Nova Allegro Analyzer (510k cleared)

    Product code: CGX. Advisory committee: Clinical Chemistry. Type: Dual Track

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoFH Industrie — JARVIS Metaphyseal Stem (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoSuzhou Sweetrich Vehicle Industry Technology Co., Ltd. — Mobility scooter (Air Classic); Mobility scooter (Air Traveller); Mobility scooter (Air Traveller2.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoMedacta International S.A. — NextAR Hip Platform (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoIotamotion, Inc. — iotaSOFT® Insertion System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoNingbo Ranor Medical Technology Co., Ltd. — Arm Blood Pressure Monitor (MJ1D,MJ1DS,MJ3D,MJ5D,MJ6D,MJ8D,RN3D,MJ4D,RN1D,RN2D) (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoUnimed Medical Supplies, Inc. — Disposable Neonatal NIBP Cuff (U1681S-C51N) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoFresenius Kabi AG — KabiHelp® Uno; KabiHelp® Advance plus (510k cleared)Fresenius Kabi USA LLC

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoSolo Pace, Inc. — Solo Pace Fusion System (SOLOFUSE1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoLiaoning Upcera Co., Ltd. — Gradual Dental Zirconia Blank - GT(F) P1, GT(F) P2, and SP Series (510k cleared)

    Product code: EIH. Advisory committee: Dental. Type: Special

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoTruvian Health — Core Metabolic (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoEthicon Endo-Surgery, LLC — ECHELON ENDOPATH Staple Line Reinforcement (ECH60R) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoInstrumentation Laboratory (IL) Co. — HemosIL Silica Clotting Time (510k cleared)

    Product code: GFO. Advisory committee: Hematology. Type: Special

    full page →fda device 510k ↗
    ›Jan 9, 2026device 510k215d agoGI Windows, Inc. — Self-Forming Magnet (Flexagon Plus OTOLoc) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 9, 2026device pma215d agoABBOTT MEDICAL — CardioMEMS™ HF System (PMA supplement)

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

    full page →fda device pma ↗
    ›Jan 9, 2026device pma215d agoEndotronix, Inc. — Cordella Pulmonary Artery Sensor System (CorPASS) (PMA supplement)

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

    full page →fda device pma ↗
    ›Jan 9, 2026device pma215d agoBoston Scientific — INGEVITY™ Family Bradycardia Leads (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ›Jan 9, 2026device pma215d agoKardium, Inc. — Globe® Catheter; Globe® Pulsed Field System (PMA supplement)Kardigan Inc

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

    full page →fda device pma ↗
    ›Jan 9, 2026device recall215d agoMedartis AG device recall (Cls II)

    Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable. — Reason: Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 9, 2026device recall215d agoFUJIFILM Healthcare Americas Corporation device recall (Cls II)

    FDR Visionary Suite; Model Number: CH-200; Version: (1) 566-16130-23, (2) 566-16130-31, (3) — Reason: It was found that the contacts of the electromagnetic contactors used inside the cabinet of the X-ray high-voltage generator were welded, and the current might continue to be supplied to the power supply circuit even if the power of the device is cut off. As a result, it cannot be denied that the circuit in question overheats and damages the surrounding parts. It may also cause smoke. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 9, 2026device recall215d agoMedartis AG device recall (Cls II)

    Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot. Component: Not applicable. — Reason: Mix up between specified lots of 2.5mm and 2.8mm outer diameter screws. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 9, 2026device recall215d agoMaquet Cardiopulmonary Gmbh device recall (Cls II)

    Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720; — Reason: Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending of the connecting cable can lead to full damage of the Venous Bubble Sensor or loose cable contact, which may trigger the errors Ven. bubble sensor defective or Ven. bubble sensor disconnected on the connected medical device. These errors can occur temporarily when the connecting cable is moved or permanently if the connection is fully compromised. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jan 9, 2026grant215d agoSANFORD RESEARCH NORTH — Momentary predictors and moderators of eating disorder behaviors and self-harm

    GM grant. $312,417. PI: Dorian R Dodd

    full page →nih reporter ↗
    ›Jan 9, 2026grant215d agoUNIVERSITY OF TOLEDO HEALTH SCI CAMPUS — Influence of arginine on Klebsiella pneumoniae mucoidy and pathogenesis

    AI grant. $39,066. PI: Brooke Ring

    full page →nih reporter ↗
    ›Jan 11, 2026device 510k213d agoAlphatec Spine, Inc. — SafeOp 3: Neural Informatix System (510k cleared)

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

    full page →fda device 510k ↗

    Week of Jan 12, 2026

    17
    ›Jan 12, 2026approval212d agoOXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN) — FDA approvalIGC Pharma, Inc.

    Sponsor: NOVEL LABS INC. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Jan 12, 2026approval
    ← prev
    page 2 of 200
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    212d ago
    TOPIRAMATE — FDA approvaltopiramate ER

    Sponsor: ASCENT PHARMS INC. Form: CAPSULE, EXTENDED RELEASE. Route: ORAL

    full page →topiramate ER →fda approvals ↗
    ›Jan 12, 2026approval212d agoFLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE (FLUTICASONE PROPIONATE) — FDA approvalFougera Pharmaceuticals Inc

    Sponsor: RESPIRENT PHARMS. Form: POWDER. Route: INHALATION

    full page →fda approvals ↗
    ›Jan 12, 2026approval212d agoACETAZOLAMIDE — FDA approvalACETAZOLAMIDE

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

    full page →ACETAZOLAMIDE →fda approvals ↗
    ›Jan 12, 2026approval212d agoCEREZYME (IMIGLUCERASE) — FDA approvalimiglucerase

    Sponsor: GENZYME. Form: INJECTABLE. Route: INJECTION

    full page →imiglucerase →fda approvals ↗
    ›Jan 12, 2026approval212d agoZYCUBO (COPPER HISTIDINATE) — FDA approvalcopper histidinate

    Sponsor: SENTYNL THERAPS INC. Form: POWDER. Route: SUBCUTANEOUS

    full page →copper histidinate →fda approvals ↗
    ›Jan 12, 2026device 510k212d agoArthrex, Inc. — Arthrex Anatomic Lapidus Plates and I-Beam Lapidus Plates (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoPromethean Restorative, LLC — DYNAMIS™ Navigation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoFoshan Topmed Dental Co., Ltd. — Dental air-motor handpiece (TM-203B2, TM-203M4, TM-205B2, TM-205M4, TM-IS, TM-ES, TM-SG20, TM-X25, TM-BB, TM-IC, TM-RA41) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoEmpower Ride, LLC — EmpowerRide NAVIGATOR (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoFoshan Topmed Dental Co., Ltd. — High speed air turbine handpiece (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoBeatles Medical Supplies (Xiantao) Co., Ltd. — Disposable Surgical Face Mask (3P00B, C2900) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoDentalez, Inc., Stardental Division — Star E900 Electric System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoShenzhen Hingmed Medical Instrument Co., Ltd. — Clinical Automatic Blood Pressure Monitor (DBP-20,DBP-20i) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoSioxmed, LLC — SBC1 Cream (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoBoston Aesthetics, Inc. — Boston iFace (Boston iFace) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 12, 2026device 510k212d agoPrecision AI Pty, Ltd. — Precision AI Surgical Planning System (PAI-SPS) (510k cleared)

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

    full page →fda device 510k ↗
    $BSX50.46+2.33%
    $SIGY0.04000.00%
    $ESPR
    $ESPR
    $IGC0.2670+0.41%