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18,553 catalysts · 4,728 grant · 3,609 8k filing · 2,621 approval · 2,129 device 510k · 1,725 device recall · 1,490 device pma

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  • grant4,728
  • 8k filing3,609
  • approval2,621
  • device 510k2,129
  • device recall1,725
  • device pma1,490
device adverse event
1,000
  • recall586
  • earnings585
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Sep 8, 2025

    50
    ›Sep 11, 2025grant355d agoUNIVERSITY OF CALIFORNIA, SAN FRANCISCO — Lumbricus terrestris erythrocruorin (LtEc) as a red blood cell substitute in ...University of California San Francisco

    DK grant. $423,017. PI: Marshall Stoller

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoMASSACHUSETTS EYE AND EAR INFIRMARY — In-silico screen and in-vivo evaluation of FDA-approved drugs to treat noise-...Massachusetts Eye and Ear Infirmary

    DC grant. $473,749. PI: Artur Indzhykulian

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoVAST THERAPEUTICS, INC. — Nebulized ALX1 as a Treatment for Difficult Non-tuberculous Mycobacterial Lun...Vast Therapeutics Inc

    AI grant. $1,000,000. PI: Nathan Allan Stasko

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoFUNCTION THERAPEUTICS, INC. — Parmodulins without Abuse Potential for the Treatment of Neuropathic Pain

    NS grant. $499,863. PI: Christopher Dockendorff

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoADEPTRIX CORPORATION — TauTrace™: An ultrasensitive immunoassay for neurodegenerative protein biomar...

    AG grant. $499,940. PI: Vladislav Bergo

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoCOLUMBIA UNIVERSITY HEALTH SCIENCES — Defining TMJ cartilage progenitors and their regulatory niche for TMJ regener...

    DE grant. $655,455. PI: Mildred Christine Embree

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoUNIVERSITY OF WASHINGTON — Understanding Social Support Network Characteristics, Alcohol Misuse, and Pos...University of Washington

    AA grant. $3,291,402. PI: Anna E. Jaffe

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoCLEVELAND CLINIC LERNER COM-CWRU — Evaluating the adoption, implementation, and maintenance of a cervical precan...

    CA grant. $183,835. PI: Montserrat Soler

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoUNIVERSITY OF WASHINGTON — Assessment of Implementation Strategies for an Innovative Facility-Specific H...University of Washington

    HD grant. $54,594. PI: krystle perez

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoUNIVERSITY OF PITTSBURGH AT PITTSBURGH — Dynamics of oxidative DNA demethylation from duplex DNA to chromatin

    ES grant. $127,384. PI: Matthew Allen Schaich

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoUNIVERSITY OF PITTSBURGH AT PITTSBURGH — Defining high-risk genomic groups of Stenotrophomonas maltophilia

    AI grant. $481,214. PI: Yohei Doi

    full page →nih reporter ↗
    ›Sep 11, 2025grant355d agoVIRGINIA COMMONWEALTH UNIVERSITY — Dissecting the co-occurrence of alcohol use/problems and suicidal behaviors: ...Virginia Commonwealth University

    AA grant. $248,999. PI: Severine Patricia Lannoy

    full page →nih reporter ↗
    ›Sep 12, 2025device 510k354d agoSparrow Acoustics, Inc. — Stethophone Pro (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoDongguan Yanxi Technology Co., Ltd. — LED Light Therapy Mask (2311, 2344, 2457, 2458) (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoErchonia Corporation — Erchonia EVRL (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoMedShape, Inc. — DynaNail TTC Fusion System (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoShenzhen Mindray Bio-Medical Electronics Co., Ltd. — ViewMateTM Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoJupiter Endovascular — Vertex(TM) Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoShanghai United Imaging Healthcare Co., Ltd. — uWS-Angio (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoPollogen, Ltd. — Legend X Platform (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoVolta Medical — Volta AF-Xplorer II (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoEnraf-Nonius, B.V. — Compact II (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoOdin Medical Limited — CADDIE (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoBecton, Dickinson and Company — BD PhaSeal™ Optima Connecting Set (C83-O); BD PhaSeal™ Optima Spike Set (C180-O) (510k cleared)BECTON DICKINSON & CO

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoMedacta International S.A. — PowerKnot High Strength Sutures (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoTangent Endoscopy, LLC — Tangent Single-Use Digital System: Tangent Single-Use Digital Catheter and Tangent Digital Controller (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoBoston Scientific Corporation — LUX-Dx II Insertable Cardiac Monitor (M302); LUX-Dx II+ Insertable Cardiac Monitor (M312) (510k cleared)BOSTON SCIENTIFIC CORP

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoMevion Medical Systems, Inc. — S250-FIT Proton Beam Radiation Therapy Device (S250-FIT) (510k cleared)MERIT MEDICAL SYSTEMS INC

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoFujifilm Irvine Scientific — Fast Warm - NX (510k cleared)

    Product code: MQL. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoDiagnoly — FETOLY (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoBrainlab AG — Spine & Trauma Navigation Instruments (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoVivachek Biotech (Hangzhou) Co., Ltd. — Wisdiag Multi-Drug Urine Test Cup; Wisdiag Multi-Drug Urine Home Test Cup (510k cleared)Hangzhou DAC Biotech Co Ltd

    Product code: NFT. Advisory committee: Clinical Toxicology. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agoBontech Co., Ltd. — BONX805 (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device 510k354d agomibeTec GmbH — bite away two (510k cleared)

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

    full page →fda device 510k ↗
    ›Sep 12, 2025device pma354d agoCordis US Corporation — S.M.A.R.T.® CONTROL® Vascular Stent System (PMA supplement)

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

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoCordis US Corporation — S.M.A.R.T.® CONTROL® Nitinol Stent System (PMA supplement)

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

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoAtrium Medical Corp. — iCast Covered Stent System (PMA supplement)Apyx Medical Corp

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

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoTerumo Medical Corporation — MISAGO® RX Self-expanding Peripheral Stent (PMA supplement)

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

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoMedtronic Minimed, Inc. — MiniMed 780G System (PMA supplement)Medtronic USA Inc

    Supplement type: 30-Day Notice. Product code: OZP. Advisory committee: CH. Decision: OK30

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoMedtronic Minimed, Inc. — Simplera Sync Sensor, Guardian 4 Sensor (PMA supplement)Medtronic USA Inc

    Supplement type: 30-Day Notice. Product code: SFI. Advisory committee: CH. Decision: OK30

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoBerlin Heart, Inc. — EXCOR Cannula Clip (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: DSQ. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d 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 ↗
    ›Sep 12, 2025device pma354d agoEdwards Lifesciences, LLC — Edwards EVOQUE tricuspid delivery system (PMA supplement)Edwards Lifesciences Corp

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

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoCordis US Corporation — PRECISE® PRO RX Nitinol Stent System; PRECISE® PRO Transcarotid Stent System (PMA supplement)

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

    full page →fda device pma ↗
    ›Sep 12, 2025device pma354d agoMedtronic Minimed — Simplera System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MDS. Advisory committee: CH. Decision: OK30

    full page →fda device pma ↗
    ›Sep 12, 2025device recall354d agoMedtronic Perfusion Systems device recall (Cls II)

    Affinity NT Oxygenator, Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir, Product Number 541B — Reason: Medtronic identified an Affinity NT Oxygenator unit with decreased CO2 gas transfer rates that did not meet performance requirements. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 12, 2025device recall354d agoGE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING device recall (Cls II)

    Elscint SPX6; dual-head nuclear medicine gamma camera designed specifically for cardiac imaging — Reason: GE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 12, 2025device recall354d agoNoah Medical Corporation device recall (Cls II)

    Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number: GAL-001 Product Description: The Galaxy SystemTM and its accessories are intended to provide bronchoscopic visualization of and access to patient airways for diagnostic and therapeutic procedure. — Reason: Due to Users not having access to the Instructions for Use/User Manual due to it being password protected. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 12, 2025device recall354d agoUIH Technologies LLC device recall (Cls II)

    Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT ATLAS MD, Rx Only — Reason: Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 12, 2025device recall354d agoUIH Technologies LLC device recall (Cls II)

    Shanghai United Imaging Healthcare Co., Ltd. Positron Emission Tomography and Computed Tomography System Model:uMI 780 MD, Rx Only — Reason: Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement. — Status: Ongoing

    full page →fda device recalls ↗
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