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calendar

22,351 catalysts · 4,728 grant · 4,406 device 510k · 3,286 8k filing · 3,188 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k4,406
  • 8k filing3,286
  • approval3,188
  • device pma2,000
  • device recall2,000
recall
1,078
  • device adverse event1,000
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Dec 9, 2024

    50
    ›Dec 11, 2024recall611d agoRising Pharma Holding, Inc. recall (Cls II)CHINA PHARMA HOLDINGS, INC.

    Duloxetine Delayed-Release Capsules USP, 30 mg, a) 30 count (NDC 57237-018-30), b) 90 count (NDC 57237-018-90) and c) 1000 count (NDC 57237-018-99) bottles, Rx only, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ — Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 11, 2024recall611d agoMidlab Incorporated recall (Cls II)

    MAXIM Assure Antibacterial, Chloroxylenol 0.1%, Net Contents: One U.S. Gallon (3.78 L), For Industrial and Institutional Use Only, MIDLAB 140 Private Brand Way, Athens, TN 37303 — Reason: cGMP Deviations: Out of specification results for micro in hand soap products. — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 11, 2024recall611d agoRising Pharma Holding, Inc. recall (Cls II)CHINA PHARMA HOLDINGS, INC.

    Duloxetine Delayed-Release Capsules USP, 20 mg, 60 count bottles, Rx only, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ NDC 57237-017-60 — Reason: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 11, 2024recall611d agoAvKARE recall (Cls II)AvKare LLC

    Sunitinib Malate Capsules, 25 mg, 28-count bottles, Rx Only, Manufactured for: AvKARE, Pulaski, TN 38478. NDC 42291-902-28 — Reason: Labeling: Label Mix-Up — Status: Ongoing

    full page →fda recalls ↗
    ›Dec 11, 2024device 510k611d agoVarian Medical Systems — Eclipse Treatment Planning System (18.1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoMicrogenics Corporation — Alinity c Benzodiazepines Reagent Kit (510k cleared)

    Product code: JXM. Advisory committee: Clinical Toxicology. Type: Special

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoMonarch Medical Technologies — EndoTool IV (3.1) (510k cleared)Medical Care Technologies Inc.

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoRafael Medical Devices, LLC — VECTR – Video Endoscopic Carpal Tunnel Release System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoLife Spine, Inc. — Cervical Plating System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoZuriMED Technologies AG — FiberLocker System: FiberLocker Implant (SpeedPatch PET), FiberLocker Instrument (FiberLocker Instrument SN) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoZimmer, Inc. — OsseoFit Stemless Shoulder System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoTechfit Digital Surgery, Inc. — TECHFIT DISRP® System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoForeo, Inc. — FAQ™ (302) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoStryker Leibinger GmbH & Co KG — SternalPlate Expansion (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoPenumbra, Inc. — Access25™ Delivery Microcatheter (510k cleared)Penumbra Inc

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoAidoc Medical , Ltd. — BriefCase-Triage (510k cleared)

    Product code: QFM. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoZhejiang Curaway Medical Technology Co., Ltd. — Radiofrequency Generator System, Cura RF Electrode (510k cleared)Zhejiang Xinkanghe Biomedical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Dec 11, 2024device 510k611d agoTechnomed Europe — Disposable Subdermal Needle Electrode, Corkscrew (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024approval610d agoNURTEC ODT (RIMEGEPANT SULFATE) — FDA approvalrimegepant sulfate ODT

    Sponsor: PFIZER. Form: TABLET, ORALLY DISINTEGRATING. Route: ORAL

    full page →rimegepant sulfate ODT →fda approvals ↗
    ›Dec 12, 2024device 510k610d agoBredent GmbH & Co. KG — visio.lign color, visio.lign shield (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoEb Neuro S.P.A. — NExT Station; NExT Station Advanced (510k cleared)

    Product code: GWL. Advisory committee: Neurology. Type: Special

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoInfrascan, Inc. — Infrascanner Model 2500 (Model 2500) (510k cleared)

    Product code: OPT. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoGe Medical Systems Information Technologies, Inc. — Mac-Lab (AltiX AI.i); CardioLab (AltiX AI.i); ComboLab (AltiX AI.i); MLCL Client Software (AltiX AI.i) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoCmf Medicon Surgical, Inc. — Medicon Epiplating System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoPhilips Ultrasound, LLC — EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoTerragene S.A. — Terragene® Bionova® Photon Process Challenge Device with unique-point integrator (PCD225-2);Terragene® Bionova® Photon Process Challenge Device with moving-front integrator (PCD225-C) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoGeniova Technologies Sociedad Limitada — GENIOVA aligners (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoShanghai United Imaging Healthcare Co., Ltd. — uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S) (510k cleared)

    Product code: KPS. Advisory committee: Radiology. Type: Special

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoLongly Biotechnology (Wuhan) Co., Ltd. — Bioceramic Root Canal Sealer and Repair Materials (i-MTA BP) (510k cleared)Cellyan Biotechnology Co., Ltd

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoNatus Neurology Incorporated — Natus Ultrapro S100 (982A0594) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 12, 2024device 510k610d agoAqua Medical, Inc. — Aqua Medical RF Vapor Ablation System (510k cleared)AVITA Medical, Inc.

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

    full page →fda device 510k ↗
    ›Dec 13, 2024approval609d agoORKAMBI (IVACAFTOR) — FDA approval(ivacaftor + lumacaftor)

    Sponsor: VERTEX PHARMS INC. Form: GRANULE. Route: ORAL

    full page →(ivacaftor + lumacaftor) →fda approvals ↗
    ›Dec 13, 2024approval609d agoORKAMBI (IVACAFTOR) — FDA approval(ivacaftor + lumacaftor)

    Sponsor: VERTEX PHARMS INC. Form: TABLET. Route: ORAL

    full page →(ivacaftor + lumacaftor) →fda approvals ↗
    ›Dec 13, 2024approval609d agoTYENNE (TOCILIZUMAB-AAZG) — FDA approvalTYENNE

    Sponsor: FRESENIUS KABI USA. Form: INJECTABLE. Route: INTRAVENOUS

    full page →TYENNE →fda approvals ↗
    ›Dec 13, 2024approval609d agoUNLOXCYT (COSIBELIMAB-IPDL) — FDA approvalcosibelimab

    Sponsor: CHECKPOINT THERAPEUTICS INC. Form: INJECTABLE. Route: INJECTION

    full page →cosibelimab →fda approvals ↗
    ›Dec 13, 2024device 510k609d agoRadiometer Medicals Aps — ABL90 FLEX PLUS System (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoABBOTT MEDICAL — Agilis NxT Steerable Introducer Dual-Reach (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoBreas Medical AB — Vivo 1, Vivo 2 (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoBreas Medical AB — Vivo 3 (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoRemex Medical Corp. — Remex Spine Surgery Navigation Instrument (510k cleared)Medicale Corp.

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoBTL Industries, Inc. — BTL-785BNF-E (510k cleared)NL INDUSTRIES INC

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoGastro Concepts, LLC — Gastro Concepts Air Assist (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoShenzhen Ulike Smart Electronics Co., Ltd. — Ice Cooling IPL Hair Removal Device (UI20 DB, UI20 RE, UI20 GP, UI20 PW, UI20S DB, UI20S RE, UI20S PW, UI20S GP,UI20 WH, UI20 GR, UI20 BS, UI20 MP, UI20 BL, UI20 PN, UI20 BR, UI20WG, UI20S WH, UI20S GR, UI20S BS, UI20S MP) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoBiosys Biyomedikal Muhendislik San. VE Tic. A.S. — Bioscope Neuromonitor Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoHeartbeam, Inc. — HeartBeam AIMIGo(TM) System (510k cleared)HeartBeam, Inc.

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoBrainu Co., Ltd. — CAIs Sensor (CAIs-001) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoZOLL Medical Corporation — 731 Series Ventilator (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoHeidelberg Engineering GmbH — Anterion (510k cleared)

    Product code: OBO. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoVarian Medical Systems, Inc. — ARIA Radiation Therapy Management System (18.1) (510k cleared)MERIT MEDICAL SYSTEMS INC

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

    full page →fda device 510k ↗
    ›Dec 13, 2024device 510k609d agoUroviu Corporation — Uro-G HD Cystoscope (1520) (510k cleared)

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

    full page →fda device 510k ↗
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    $CPHI0.7101-0.82%
    $CPHI0.7101-0.82%
    $PEN324.29-0.11%
    $MDCE0.00020.00%
    $HKPD
    $PFE26.86+2.11%
    $VERX12.59+2.36%
    $NL6.0500-1.14%
    $BEATW
    $CCCC
    $VERX12.59+2.36%
    $MCLE
    $RCEL8.0100-1.35%
    $MMSI90.72-0.53%