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23,181 catalysts · 4,900 device 510k · 4,728 grant · 3,532 approval · 3,230 8k filing · 2,000 device pma · 2,000 device recall

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  • device 510k4,900
  • grant4,728
  • approval3,532
  • 8k filing3,230
  • device pma2,000
  • device recall2,000
recall
1,126
  • device adverse event1,000
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 25, 2024

    36
    ›Nov 27, 2024recall625d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Moberg Pharma AB

    Guaifenesin Dextromethorphan Syrup, 200 mg/20mg per 10 mL, Major Pharmaceuticals 8401 Bearing Drive, Suite 100, Indianapolis, IN, 46268, NDC 0904-7135-72 — Reason: Failed Impurity/Degradation Specifications — Status: Terminated

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoSafecor Health, LLC recall (Cls II)Aspire Biopharma Holdings, Inc.

    Aspirin Chewable tablet 81 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-129-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoSafecor Health, LLC recall (Cls II)

    Calcium Carbonate Chewable 500 mg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-106-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoTailstorm Health INC recall (Cls II)F. Hoffmann-La Roche Ltd

    BEVACIZUMAB (AVASTIN)1.25mg/0.05mL, Sterile Injection, 0.5 mL Single-Dose Syringe, Rx Only, Repackaged by: Medivant Healthcare: 24416 N 19th Ave, Phoenix, AZ, NDC 81483-0041-1 — Reason: Lack of Sterility Assurance — Status: Terminated

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

    Ramipril Capsules USP 2.5 mg, a) 90 count (NDC 68180-589-09), b) 100 count NDC 68180-589-01), and c) 500 count (NDC 68180-589-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India — Reason: CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor — Status: Terminated

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

    Ramipril Capsules USP 5 mg, a) 90 count (NDC 68180-590-09), b) 100 count NDC 68180-590-01), and c) 500 count (NDC 68180-590-02) bottles, Rx only, Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, Manufactured by Lupin Limited, Goa, India — Reason: CGMP Deviations: Active pharmaceutical ingredient was sourced from an unapproved vendor — Status: Terminated

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoSafecor Health, LLC recall (Cls II)

    Docusate Sodium 250 mg, 1 Softgel in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-101-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoNoven Pharmaceuticals Inc recall (Cls II)NRX Pharmaceuticals, Inc.

    Xelstrym (dextroamphetamine) transdermal system, 13.5 mg dextroamphetamine/9 hours, 30 individually sealed transdermal patches, inside a foil-sealed polypropylene tray, packed in a paper carton/box, MANUFACTURED BY NOVEN PHARMACEUTICALS, INC., Miami, FL 33186 United Sates, NDC 68968-0215-3 — Reason: Defective Delivery System: The product does not meet predetermined specifications for Coldflow (adhesive). — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoEvaric Pharmaceuticals Inc. recall (Cls II)Oric Pharmaceuticals, Inc.

    Lisinopril Tablets, USP 10 mg, 90 tablets per bottle, Rx Only, Distributed by: Walmart, Bentonville, AR 72716, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045, NDC# 68645-610-90. — Reason: Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet. — Status: Completed

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoSafecor Health, LLC recall (Cls II)

    Vitamin B1, 100 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-108-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 27, 2024recall625d agoSafecor Health, LLC recall (Cls II)

    Vitamin D3, 25 mcg, 1 tablet in blister card-foils, 100-count unit dose box, www.safecorhealth.com, NDC 48433-104-01 — Reason: cGMP Deviations: Observations were made that some blister card-foils were separating from the blister cavity. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 27, 2024device 510k625d agoNextbiomedical Co., Ltd. — Nexpowder (510k cleared)ACRO BIOMEDICAL CO., LTD.

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoDeka Research & Development Corp. — Remunity System (510k cleared)

    Product code: QJY. Advisory committee: General Hospital. Type: Special

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoEizo Corporation — RadiForce RX570; RadiForce RX570-AR (510k cleared)

    Product code: PGY. Advisory committee: Radiology. Type: Abbreviated

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoOntact Health Co., Ltd. — Sonix Health (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoSamsung Medison Co., Ltd. — HERA W10 Diagnostic Ultrasound System; HERA W9 Diagnostic Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoEasymed Instruments Co., Ltd. — Pelvic Floor Stimulator (Intrelief PFE) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoShenzhen Walton Technology Co., Ltd. — LED Light Therapy Machine (G1, G3, G4, G6) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoCyden Limited — SmoothSkin Pure Switch (SSC1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoKarl Storz SE & CO. KG — KARL STORZ Pediatric Cysto-Urethro-Fiberscope (11274BCU1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoVilex, LLC — TACTIX Vector Syndesmosis System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoCeragem Co., Ltd. — Ceragem Automatic Thermal Massager (CGM-MB-1902) (510k cleared)

    Product code: JFB. Advisory committee: Physical Medicine. Type: Special

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoPrevest Denpro Limited — C&B Ceramic; C&B Permanent; C&B Interim (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoCellmyx — AirSculpt Body Contouring System (AIRS-1-SYS) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoSharkninja Operating, LLC — CryoGlow (FW3XXXX) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoBard Access Systems, Inc. — PowerLoc™ Max Power Injectable Infusion Set; SafeStep™ Huber Needle Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoSpectrum Vascular — SV Spectrum MRC Central Venous Catheter; SV Spectrum MR Central Venous Catheter; SV Central Venous Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoConmed Corporation — BioBrace® (510k cleared)CONMED Corp

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

    full page →fda device 510k ↗
    ›Nov 27, 2024device 510k625d agoZhejiang Zhonglei Medical Technology Co. , Ltd. — Power wheelchair (510k cleared)Zhejiang Xinkanghe Biomedical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Nov 29, 2024approval623d agoYESINTEK (USTEKINUMAB-KFCE) — FDA approvalustekinumab biosimilar

    Sponsor: BIOCON BIOLOGICS INC. Form: INJECTABLE. Route: INJECTION

    full page →ustekinumab biosimilar →fda approvals ↗
    ›Nov 29, 2024approval623d agoDAYTRANA (METHYLPHENIDATE) — FDA approvalNoven Pharmaceuticals Inc

    Sponsor: NOVEN PHARMS INC. Form: FILM, EXTENDED RELEASE. Route: TRANSDERMAL

    full page →fda approvals ↗
    ›Nov 29, 2024approval623d agoXELSTRYM (DEXTROAMPHETAMINE) — FDA approvalNoven Pharmaceuticals Inc

    Sponsor: NOVEN PHARMS INC. Form: SYSTEM. Route: TRANSDERMAL

    full page →fda approvals ↗
    ›Nov 29, 2024device 510k623d agoSurgical Instrument Service and Savings, Inc. — Medline ReNewal Reprocessed Abbott Inquiry Steerable Diagnostic Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 29, 2024device 510k623d agoMovano Inc. Dba Movano Health — Evie Med Ring (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 29, 2024device 510k623d agoRuthless, LLC Dba Ruthless Spine — Ruthless Spine RJB (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 29, 2024device 510k623d agoMedical Electronic Systems , Ltd. — YO Home Sperm Test (510k cleared)

    Product code: POV. Advisory committee: Hematology. Type: Traditional

    full page →fda device 510k ↗

    Week of Dec 2, 2024

    14
    ›Dec 2, 2024approval620d agoTECVAYLI (TECLISTAMAB-CQYV) — FDA approvalteclistamab

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →teclistamab →fda approvals ↗
    ›Dec 2, 2024approval
    ← prev
    page 18 of 464
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    620d ago
    TALVEY (TALQUETAMAB-TGVS) — FDA approvaltalquetamab

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →talquetamab →fda approvals ↗
    ›Dec 2, 2024approval620d agoAXTLE (PEMETREXED DIPOTASSIUM) — FDA approvalAXTLE

    Sponsor: AVYXA HOLDINGS. Form: POWDER. Route: INTRAVENOUS

    full page →AXTLE →fda approvals ↗
    ›Dec 2, 2024device 510k620d agoFlight Medical Innovations , Ltd. — Ventoux VC2; Ventoux VC3 (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 2, 2024device 510k620d agoMicro Therapeutics, Inc. d/b/a ev3 Neurovascular — Riptide™ Aspiration Pump; Riptide™ Collection Canister with Intermediate Tubing (510k cleared)

    Product code: JCX. Advisory committee: General, Plastic Surgery. Type: Special

    full page →fda device 510k ↗
    ›Dec 2, 2024device 510k620d agoPhilips Medical Systems Nederland B.V. — Philips IntelliSite Pathology Solution (510k cleared)

    Product code: PSY. Advisory committee: Pathology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 2, 2024device 510k620d agoSynthon Hispania S.L. — GripMate (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 2, 2024device 510k620d agoApira Science, Inc. — GroWell BT Hair Growth System (GW10042) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 2, 2024device 510k620d agoSTERIS Corporation — enspire 3000 Cleaning and Liquid Chemical Sterilant Processing System (510k cleared)STERIS plc

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

    full page →fda device 510k ↗
    ›Dec 2, 2024device 510k620d agoIntravu, Inc. — MIDASVu (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 2, 2024device 510k620d agoVilex, LLC — Hintermann Series H2 Total Ankle System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 3, 2024approval619d agoBOSULIF (BOSUTINIB MONOHYDRATE) — FDA approvalAlembic Pharmaceuticals Inc

    Sponsor: PF PRISM CV. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Dec 3, 2024approval619d agoBOSULIF (BOSUTINIB MONOHYDRATE) — FDA approvalAlembic Pharmaceuticals Inc

    Sponsor: PF PRISM CV. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Dec 3, 2024approval619d agoVABOMERE (MEROPENEM) — FDA approvalHQ Speciality Pharma

    Sponsor: REMPEX. Form: POWDER. Route: INTRAVENOUS

    full page →fda approvals ↗
    $NRXP
    $ASBP
    $LBRX45.02-0.79%
    $FRTRY
    $ACBM
    $HCWB
    $ORIC13.75+0.15%
    $CNMD32.58+1.46%
    $LBRX45.02-0.79%
    $STE235.15-0.61%