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calendar

14,388 catalysts · 3,350 8k filing · 2,435 grant · 2,379 approval · 1,691 device 510k · 1,229 device recall · 1,158 device pma

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  • 8k filing3,350
  • grant2,435
  • approval2,379
  • device 510k1,691
  • device recall1,229
  • device pma1,158
device adverse event
1,000
  • earnings584
  • recall481
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Oct 13, 2025

    50
    ›Oct 13, 2025device recall306d agoTMJ Solutions Inc device recall (Cls I)TIC Solutions, Inc.

    TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only — Reason: Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 14, 2025approval305d agoWEGOVY (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoSAXENDA (LIRAGLUTIDE) — FDA approvalNovo Nordisk Inc

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoXULTOPHY 100/3.6 (INSULIN DEGLUDEC) — FDA approvalNovo Nordisk Inc

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoEPINEPHRINE — FDA approvaladrenaline

    Sponsor: AMNEAL. Form: SOLUTION. Route: INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS

    full page →adrenaline →fda approvals ↗
    ›Oct 14, 2025approval305d agoVICTOZA (LIRAGLUTIDE) — FDA approvalSaxenda

    Sponsor: NOVO NORDISK INC. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →Saxenda →fda approvals ↗
    ›Oct 14, 2025approval305d agoOZEMPIC (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025approval305d agoOZEMPIC (SEMAGLUTIDE) — FDA approvalNovo Nordisk AS

    Sponsor: NOVO. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 14, 2025device 510k305d agoResponsive Arthroscopy, LLC — Mini Superhawk Suture Anchor System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoDawell Medical, LLC — Lithoblast Single Use Holmium Laser Fibers (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoAsset Medikal — FlowArt® Vial Access Device Vented (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoShenzhen Qiaochengli Technology Co., Ltd. — IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoPureway Compliance, Inc. — PureWay Sharps Container 1-Gal, 2-Gal, 3-Gal (800011 800012, 800013) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoPhysio-Control, Inc. — LIFEPAK 15 AC Power Adapter (41577-000333) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoNexus Spine — PressON Spinal Fixation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoRapid Nexus Nanotech Wound Solutions, Inc. — Hemastyl(™) Wound Dressing (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoKeter Canada, Inc. — Community Containers (Flap and Daisy) (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device 510k305d agoMeta Systems Co., Ltd. — Demi Pro (510k cleared)

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

    full page →fda device 510k ↗
    ›Oct 14, 2025device pma305d agoShockwave Medical, Inc. — Shockwave™ lntravascular Lithotripsy {IVL) System with Shockwave C2/ C2+/ C2 Aero Coronary IVL Catheter (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 14, 2025device pma305d agoPhysio-Control, Inc. — LIFEPAK 1000 defibrillator (PMA supplement)

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

    full page →fda device pma ↗
    ›Oct 14, 2025device pma305d agoAdvanced Bionics — HiResolution™ Bionic Ear System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MCM. Advisory committee: EN. Decision: OK30

    full page →fda device pma ↗
    ›Oct 14, 2025device recall305d agoBecton Dickinson & Company device recall (Cls II)BECTON DICKINSON & CO

    BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341; — Reason: BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 14, 2025device recall305d agoOlympus Corporation of the Americas device recall (Cls II)

    Brand Name: EVIS EXERA III Duodenovideoscope Product Name: Olympus TJF-Q190V Model/Catalog Number: TJF-Q190V Product Description: This instrument is intended to be used with an Olympus video system center, light source, documentation equipment, monitor, EndoTherapy accessories (such as a biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery. — Reason: Continued reports of positive cultures and infections have identified updates to the reprocessing materials to minimize potential deviations in TJF duodenoscope reprocessing. Olympus is informing users of these changes, reminding users to closely follow the operation and reprocessing instructions, and providing updated materials to users. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 14, 2025device recall305d agoBeckman Coulter Ireland, Inc. device recall (Cls II)

    BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitative determination of Bicarbonate in human serum and plasma on Beckman Coulter AU analyzers. — Reason: Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample. — Status: Ongoing

    full page →fda device recalls ↗
    ›Oct 15, 2025approval304d agoCELECOXIB — FDA approvalCelebrex

    Sponsor: YILING. Form: CAPSULE. Route: ORAL

    full page →Celebrex →fda approvals ↗
    ›Oct 15, 2025approval304d agoCELECOXIB — FDA approvalCelebrex

    Sponsor: YILING. Form: CAPSULE. Route: ORAL

    full page →Celebrex →fda approvals ↗
    ›Oct 15, 2025approval304d agoFINTEPLA (FENFLURAMINE HYDROCHLORIDE) — FDA approvalfenfluramine hydrochloride

    Sponsor: UCB INC. Form: SOLUTION. Route: ORAL

    full page →fenfluramine hydrochloride →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoLACOSAMIDE — FDA approvalLACOSAMIDE

    Sponsor: HETERO LABS LTD V. Form: TABLET. Route: ORAL

    full page →LACOSAMIDE →fda approvals ↗
    ›Oct 15, 2025approval304d agoCONJUGATED ESTROGENS (ESTROGENS, CONJUGATED) — FDA approvalIngenus Pharmaceuticals LLC

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

    full page →fda approvals ↗
    ›Oct 15, 2025approval304d agoCONJUGATED ESTROGENS (ESTROGENS, CONJUGATED) — FDA approvalIngenus Pharmaceuticals LLC

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

    full page →fda approvals ↗
    ›Oct 15, 2025approval304d ago— FDA approvalMerck Sharp & Dohme LLC

    Sponsor: MERCK SHARP AND DOHME LLC

    full page →fda approvals ↗
    ›Oct 15, 2025approval304d agoLYTGOBI (FUTIBATINIB) — FDA approvalfutibatinib

    Sponsor: TAIHO ONCOLOGY. Form: TABLET. Route: ORAL

    full page →futibatinib →fda approvals ↗
    ›Oct 15, 2025approval304d agoPANTOPRAZOLE SODIUM — FDA approvalPANTOPRAZOLE SODIUM

    Sponsor: ASPIRO. Form: INJECTABLE. Route: INTRAVENOUS

    full page →PANTOPRAZOLE SODIUM →fda approvals ↗
    ›Oct 15, 2025approval304d agoPANTOPRAZOLE SODIUM — FDA approvalPANTOPRAZOLE SODIUM

    Sponsor: ASPIRO. Form: INJECTABLE. Route: INTRAVENOUS

    full page →PANTOPRAZOLE SODIUM →fda approvals ↗
    ›Oct 15, 2025approval304d agoAMLODIPINE BESYLATE AND VALSARTAN (AMLODIPINE BESYLATE) — FDA approvalamlodipine besylate

    Sponsor: TORRENT. Form: TABLET. Route: ORAL

    full page →amlodipine besylate →fda approvals ↗
    ›Oct 15, 2025approval304d agoAMLODIPINE BESYLATE AND VALSARTAN (AMLODIPINE BESYLATE) — FDA approvalamlodipine besylate

    Sponsor: TORRENT. Form: TABLET. Route: ORAL

    full page →amlodipine besylate →fda approvals ↗
    ›Oct 15, 2025approval304d agoLIRAGLUTIDE — FDA approvalNovo Nordisk Inc

    Sponsor: NANJING KING FRIEND. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →fda approvals ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)

    Reconstitution XO Solution for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health a) 5% Exosomes, 10 mL vial and b) 10% Exosomes, 5 mL vial, Extension Health a) 20% Exosomes, 10 mL vial, b) 10% Exosomes, 10 mL vial and Medical Health Institute (MHI), a) 10 % Exosomes, 2mL vial, 5mL vial, 10mL vial, b) 5% Exosomes, 2mL vial, 5mL vial, 10mL vial. — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)Baylor College of Medicine

    Glycine for Injection, all strengths and presentations, GenoGenix LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)

    GHK-Cu (Copper Peptide) for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)Tsuno Rice Fine Chemicals Co Ltd

    Magnesium Chloride for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)EVER Neuro Pharma GmbH

    Cerebrolysin for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)

    L-Carnitine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692 — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)Baudax Bio Inc

    N-Acetyl-L-Cysteine for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)

    NAD+ (Nicotinamide adenine dinucleotide), a) 50 mg/mL, b) 100 mg/mL, 10 mL multi-dose vials, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. Also labeled as manufactured for CELIA Health — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
    ›Oct 15, 2025recall304d agoGenoGenix LLC recall (Cls II)Nexus Pharmaceuticals Inc

    Methylene Blue for Injection, all strengths and presentations, GenoGenix, LLC, 2840 NW 2nd Ave Ste 204 Boca Raton, FL 33431-6692. — Reason: Lack of Assurance of Sterility — Status: Ongoing

    full page →fda recalls ↗
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