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9,481 catalysts · 3,350 8k filing · 2,029 grant · 1,000 device adverse event · 897 approval · 659 device 510k · 584 earnings

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  • 8k filing3,350
  • grant2,029
  • device adverse event1,000
  • approval897
  • device 510k659
  • earnings584
device pma
503
  • device recall211
  • phase 2 completion172
  • recall167
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Mar 2, 2026

    50
    ›Mar 4, 2026device 510k165d agoLifevac, LLC — LifeVac (510k cleared)

    Product code: QXN. Advisory committee: Ear, Nose, Throat. Type: Direct

    full page →fda device 510k ↗
    ›Mar 4, 2026device 510k165d agoGlobalcare Medical Technology Co., Ltd. — TENS/EMS device (GUSE01) (510k cleared)NewBay Medical Technology Co Ltd

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

    full page →fda device 510k ↗
    ›Mar 4, 2026device 510k165d agoDentis Co., Ltd. — Dentis SQ-SL AXEL Fixture (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 4, 2026device 510k165d agoDentsply Sirona, Inc. — SureSmile Software (510k cleared)DENTSPLY SIRONA Inc.

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

    full page →fda device 510k ↗
    ›Mar 4, 2026device 510k165d agoSuzhou Master Machinery Manufacturing Co.,Ltd — Electric Wheelchair (MP148) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 4, 2026device 510k165d agoQT Imaging Holdings, Inc. — QT Scanner 2000 Model A (510k cleared)QT IMAGING HOLDINGS, INC.

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

    full page →fda device 510k ↗
    ›Mar 4, 2026device 510k165d agoRadcliffe Watts, LLC — Klär Lite (RCW-KL1000) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 4, 2026device 510k165d agoOsstem Implant Co., Ltd. — Healing Abutment System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 4, 2026device pma165d 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 ↗
    ›Mar 4, 2026device pma165d agoABBOTT MEDICAL — HeartMate 3™ Left Ventricular Assist System (PMA supplement)

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

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoMedtronic Cardiac Rhythm Disease Management — Cobalt MRI CRT-D (DTPB2Dl, DTPB2D4, DTPB2Ql, DTPB2QQ); Cobalt XT MRI CRT-D (DTPA2Dl, DTPA2D4, DTPA2Ql, DTPA2QQ); Crome M (PMA supplement)

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

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoElement Science, Inc. — Jewel Patch Wearable Cardioverter Defibrillator (P-WCD) (Jewel); Jewel P-WCD Firmware; Jewel Placement Accessory (Class (PMA supplement)

    Supplement type: Real-Time Process. Product code: MVK. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoMedtronic Cardiac Rhythm Disease Management — Cobalt MRI ICD (DDPB3Dl, DDPB3D4, DVPB3Dl, DVPB3D4); Cobalt XT MRI ICD (DDPA2Dl, DDPA2D4, DVPA2Dl, DVPA2D4); Crome MRI I (PMA supplement)

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

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoSTAAR Surgical Company — The EVO/EVO+ Visian Implantable Collamer Lens (ICL) (PMA supplement)STAAR SURGICAL CO

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

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoLife Technologies Corporation — Oncomine™ Dx Target Test (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: PQP. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoABBOTT MEDICAL — HeartMate 3™ Left Ventricular Assist System (PMA supplement)

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

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoCooperVision, Inc. — Biofinity Toric (comfilcon A) Soft (Hydrophilic) Contact Lenses for Extended Wear (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LPM. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Mar 4, 2026device pma165d agoCooperVision, Inc. — Biofinity Toric Multifocal (comfilcon A) Soft (Hydrophilic) Contact Lenses for Extended Wear (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LPM. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Mar 4, 2026device recall165d agoKoven Technology, Inc. device recall (Cls II)WM TECHNOLOGY, INC.

    Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector with LCD numeric display, used with interchangeable probes to detect vascular blood-flow signals and display heart rate; affected units were packaged with a 2 MHz BT2M20S8C fetal probe and labeled for both vascular and fetal applications. — Reason: Product labeling includes a fetal indication for use that is not cleared under its 510(k). — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 4, 2026grant165d agoGORDON RESEARCH CONFERENCES — 2026 Single-Cell Cancer Biology Gordon Research Conference and Gordon Researc...

    CA grant. $10,000. PI: Ken Chen

    full page →nih reporter ↗
    ›Mar 4, 2026grant165d agoALBERT EINSTEIN COLLEGE OF MEDICINE — Scalable imaging approach to measure muscle bioenergetics in CKD.Albert Einstein College of Medicine

    AR grant. $556,651. PI: Matthew K Abramowitz

    full page →nih reporter ↗
    ›Mar 4, 2026grant165d agoUNIVERSITY OF ALABAMA AT BIRMINGHAM — 10-Year Follow-Up of the Medical Optimization and Management of Pregnancies w...

    DK grant. $1,934,914. PI: Ashley Nicole Battarbee

    full page →nih reporter ↗
    ›Mar 4, 2026grant165d agoUNIVERSITY OF MICHIGAN AT ANN ARBOR — Neocortical-hippocampal coordination and plasticity in sleep-dependent memory...

    NS grant. $419,920. PI: SARA J ATON

    full page →nih reporter ↗
    ›Mar 5, 2026approval164d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalPrinston Pharmaceutical Inc

    Sponsor: TEVA. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Mar 5, 2026approval164d agoCHOLESTYRAMINE — FDA approvalCHOLESTYRAMINE

    Sponsor: MICRO LABS. Form: POWDER. Route: ORAL

    full page →CHOLESTYRAMINE →fda approvals ↗
    ›Mar 5, 2026approval164d agoIBUPROFEN — FDA approvalMidol

    Sponsor: RUBICON RESEARCH. Form: SUSPENSION. Route: ORAL

    full page →Midol →fda approvals ↗
    ›Mar 5, 2026approval164d agoTECVAYLI (TECLISTAMAB-CQYV) — FDA approvalteclistamab

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

    full page →teclistamab →fda approvals ↗
    ›Mar 5, 2026approval164d agoTALVEY (TALQUETAMAB-TGVS) — FDA approvaltalquetamab

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

    full page →talquetamab →fda approvals ↗
    ›Mar 5, 2026approval164d agoOLANZAPINE — FDA approvalTEVA PHARMACEUTICAL INDUSTRIES LTD

    Sponsor: ANTHEA PHARMA. Form: POWDER. Route: INTRAMUSCULAR

    full page →fda approvals ↗
    ›Mar 5, 2026approval164d agoAPREPITANT — FDA approvalAPREPITANT

    Sponsor: MYLAN. Form: EMULSION. Route: INTRAVENOUS

    full page →APREPITANT →fda approvals ↗
    ›Mar 5, 2026approval164d agoCHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE (AMITRIPTYLINE HYDROCHLORIDE) — FDA approvalAlgoTherapeutix SAS

    Sponsor: TP ANDA HOLDINGS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Mar 5, 2026approval164d agoCHLORDIAZEPOXIDE AND AMITRIPTYLINE HYDROCHLORIDE (AMITRIPTYLINE HYDROCHLORIDE) — FDA approvalAlgoTherapeutix SAS

    Sponsor: TP ANDA HOLDINGS. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Mar 5, 2026approval164d agoXYZAL ALLERGY 24HR (LEVOCETIRIZINE DIHYDROCHLORIDE) — FDA approvalSanofi

    Sponsor: CHATTEM SANOFI. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Mar 5, 2026approval164d agoKEFLEX (CEPHALEXIN) — FDA approvalBelcher Pharmaceuticals LLC

    Sponsor: PRAGMA. Form: FOR SUSPENSION. Route: ORAL

    full page →fda approvals ↗
    ›Mar 5, 2026approval164d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

    Sponsor: PRINSTON INC. Form: TABLET. Route: ORAL

    full page →ALDACTAZIDE →fda approvals ↗
    ›Mar 5, 2026approval164d agoERLEADA (APALUTAMIDE) — FDA approvalapalutamide

    Sponsor: JANSSEN BIOTECH. Form: TABLET. Route: ORAL

    full page →apalutamide →fda approvals ↗
    ›Mar 5, 2026approval164d agoPAROXETINE HYDROCHLORIDE — FDA approvalPAROXETINE HYDROCHLORIDE

    Sponsor: ANNORA PHARMA. Form: SUSPENSION. Route: ORAL

    full page →PAROXETINE HYDROCHLORIDE →fda approvals ↗
    ›Mar 5, 2026device 510k164d agoZhuhai DR Medical Instruments Co., Ltd. — Extension tube (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoParagon 28, Inc. — Phantom® Hindfoot TTC/TC Nail System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoNanosonics Limited — CORIS System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoEarlitec Diagnostics — EarliPoint Assessment (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoIvoclar Vivadent, Inc. — Adhese 2 (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoArthrex, Inc. — Arthrex FibuLock Nail System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoPhilips Medical Systems Nederland B.V. — AV Cardiac CT (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoOrca Dental AI , Ltd. — CEPHX3D (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoJiangsu Yuyue Medical Equipment & Supply Co., Ltd. — YUWELL® Electronic Blood Pressure Monitor (YE630CR) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device 510k164d agoEsaote, S.p.A. — Magnifico Open (100009900) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 5, 2026device pma164d agoBiotronik, Inc. — Acticor Sky VR-T (481989); Rivacor Sky VR-T (481984); Rivacor Rise VR-T (482020); Rivacor Aura VR-T (482015); Acticor Sk (PMA supplement)

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

    full page →fda device pma ↗
    ›Mar 5, 2026device pma164d agoShockwave Medical, Inc. — Shockwave™ lntravascular Lithotripsy (IVL) System with Shockwave 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 ↗
    ›Mar 5, 2026device pma164d agoBoston Scientific Corp — ROTAPRO™ Rotational Atherectomy System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
    ← prev
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    $XRAY11.59+0.09%
    $SNY43.72-0.14%
    $TEVA36.77+0.68%
    $STAA26.18+3.36%
    $MAPS0.4170+1.46%
    $QTIWW0.1500-18.92%
    $BSX51.83+0.27%