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12,031 catalysts · 3,350 8k filing · 2,283 grant · 1,778 approval · 1,169 device 510k · 1,000 device adverse event · 849 device pma

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  • 8k filing3,350
  • grant2,283
  • approval1,778
  • device 510k1,169
  • device adverse event1,000
  • device pma849
device recall
655
  • earnings584
  • recall282
  • phase 2 completion172
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    • Oncology148
    • Infectious Disease46
    • Cardiology37
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    Week of Dec 15, 2025

    50
    ›Dec 15, 2025device recall244d agoDiagnostica Stago, Inc. device recall (Cls II)

    Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (PF4) antibodies generated during the type II heparin-induced thrombocytopenia (HIT type II) by ELISA. — Reason: Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/10; Model Number: 722029; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    ICU Medical Plum Duo Precision IV Pump, List Numbers: 400020403 (US), 400021003 (Philippines) — Reason: Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoSunMed Holdings, LLC device recall (Cls I)Sagent Pharmaceuticals Inc

    Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer Model/Catalog Number: 7730ALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No — Reason: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10; Model Number: 722010; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoSysmex America, Inc. device recall (Cls II)

    TS-10/TS-10H Tube Sorter, automatic sorting system for sorting barcoded sample tubes, Catalog Number BN168792, running software versions 00-17 — Reason: Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20 Biplane; Model Number: 722008; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoSunMed Holdings, LLC device recall (Cls I)Sagent Pharmaceuticals Inc

    Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: no — Reason: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    Plum Duo Infusion System, List Number 40002-04-01 — Reason: ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in your Plum Duo Infusion Pump fails, the pump may not produce audible alarms, alerts, or provide audible feedback for touchscreen inputs. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoSunMed Holdings, LLC device recall (Cls I)Sagent Pharmaceuticals Inc

    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No — Reason: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoHologic, Inc device recall (Cls II)

    Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument. — Reason: Presence of particulates in affected devices that can be deposited into breast tissue during use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20 OR Table; Model Number: 722023; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20 Biplane; Model Number: 722013; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoWilson-Cook Medical Inc. device recall (Cls II)

    Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10 — Reason: Nasal feeding tube packaged without the nasal transfer tube component. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10; Model Number: 722026; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall244d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20; Model Number: 722006; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025grant244d agoJACKSON LABORATORY — Genetic dissection of microglia functions in complement-mediated synapse loss...

    AG grant. $716,579. PI: Erik Bradley Bloss

    full page →nih reporter ↗
    ›Dec 15, 2025grant244d agoUNIVERSITY OF VIRGINIA — Model-Based Syllabic Prediction in the Avian Auditory PalliumUniversity of Virginia

    DC grant. $41,394. PI: Bao Le

    full page →nih reporter ↗
    ›Dec 15, 2025grant244d agoRUTGERS BIOMEDICAL AND HEALTH SCIENCES — The Role of APP-metabolites on Extracellular Vesicle Cargo and Function

    AG grant. $639,838. PI: MARC D TAMBINI

    full page →nih reporter ↗
    ›Dec 15, 2025grant244d agoCLEVELAND CLINIC LERNER COM-CWRU — Endothelial TLR2/4 signaling in sex dimorphism of pathological angiogenesis a...

    AG grant. $659,309. PI: Tatiana V Byzova

    full page →nih reporter ↗
    ›Dec 15, 2025grant244d agoUNIVERSITY OF MISSOURI-COLUMBIA — Targeting LARP6 in aging-associated heart failure

    AG grant. $429,394. PI: Shawn Brady Bender

    full page →nih reporter ↗
    ›Dec 16, 2025approval243d agoTIZANIDINE HYDROCHLORIDE — FDA approvalTIZANIDINE HYDROCHLORIDE

    Sponsor: APOTEX INC. Form: CAPSULE. Route: ORAL

    full page →TIZANIDINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 16, 2025approval243d agoHYMPAVZI (MARSTACIMAB-HNCQ) — FDA approvalmarstacimab

    Sponsor: PFIZER INC. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →marstacimab →fda approvals ↗
    ›Dec 16, 2025approval243d agoEXDENSUR (DEPEMOKIMAB-ULAA) — FDA approvaldepemokimab

    Sponsor: GLAXOSMITHKLINE LLC. Form: INJECTION

    full page →depemokimab →fda approvals ↗
    ›Dec 16, 2025approval243d agoHYDROXYZINE HYDROCHLORIDE — FDA approvalHYDROXYZINE HYDROCHLORIDE

    Sponsor: NOVITIUM PHARMA. Form: SYRUP. Route: ORAL

    full page →HYDROXYZINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 16, 2025approval243d agoFLUTICASONE PROPIONATE — FDA approvalFluticasone Propionate Glenmark

    Sponsor: AUROBINDO PHARMA LTD. Form: SPRAY, METERED. Route: NASAL

    full page →Fluticasone Propionate Glenmark →fda approvals ↗
    ›Dec 16, 2025approval243d agoLOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalAlembic Pharmaceuticals Inc

    Sponsor: ALEMBIC PHARMS LTD. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Dec 16, 2025approval243d agoCARIPRAZINE HYDROCHLORIDE — FDA approvalCARIPRAZINE HYDROCHLORIDE

    Sponsor: AUROBINDO PHARMA LTD. Form: CAPSULE. Route: ORAL

    full page →CARIPRAZINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 16, 2025approval243d agoVYBRIQUE (SILDENAFIL CITRATE) — FDA approvalRevatio

    Sponsor: IBSA. Form: FILM. Route: ORAL

    full page →Revatio →fda approvals ↗
    ›Dec 16, 2025approval243d agoLOSARTAN POTASSIUM — FDA approvalLOSARTAN POTASSIUM

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

    full page →LOSARTAN POTASSIUM →fda approvals ↗
    ›Dec 16, 2025approval243d agoBECLOMETHASONE DIPROPIONATE — FDA approvalSOLIGENIX, INC.

    Sponsor: AMNEAL IRELAND LTD. Form: AEROSOL, METERED. Route: INHALATION

    full page →fda approvals ↗
    ›Dec 16, 2025approval243d agoLOSARTAN POTASSIUM — FDA approvalAlembic Pharmaceuticals Inc

    Sponsor: ALEMBIC PHARMS LTD. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Dec 16, 2025device 510k243d agoFujirebio Diagnostics,Inc. — ADVIA Centaur Cytokeratin Fragment 21-1 (510k cleared)Co-Diagnostics, Inc.

    Product code: OVK. Advisory committee: Immunology. Type: Traditional

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoPentax of America, Inc. — PENTAX Medical Video Upper GI Scopes (EG Family) (EG Family); PENTAX Medical Video Colonoscopes (EC Family) (EC Family) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoIntuitive Surgical, Inc. — IRISeg (510k cleared)INTUITIVE SURGICAL INC

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoBaxter Healthcare Corporation — Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) (510k cleared)Baxter Healthcare Corp

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoSpectrum Vascular — BioFlo Hybrid PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology and PASV Valve Technology; BioFlo PICC with ENDEXO Technology; BioFlo Midline Catheter; Xcela Power Injectable PICC; Xcela PICC with PASV Valve Technology; Xcela Hybrid PICC with PASV Valve Technology (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoCmr Surgical Limited — Versius Surgical System (Versius Plus) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoZhejiang Geyi Medical Instrument Co., Ltd. — Single-use Digital Flexible Ureteroscope (GY-UR9.3); Single-use Digital Flexible Ureteroscope (GY-UR8.4); Single-use Digital Flexible Ureteroscope (GY-UR7.5); Endoscope camera system (GY-AIO-121) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoGordian Surgical, Ltd. — TroClose 1200 (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoGuangzhou Red Pine Medical Instrument Co., Ltd. — Single-Use Video Flexible Ureterorenoscope (RP-U-C03R9, RP-U-C03R3, RP-U-C03S9, RP-U-C03S3); Endoscopic Video Image Processor (RP-IPD-V2000EF); Endoscopic Video Image Processor (RP-IPD-V1000F) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoSignature Orthopaedics Pty, Ltd. — Cambridge Partial Knee (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoSkanray Technologies Limited — SKAN C PULSAR (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoProlaio, Inc. — prolaio eVO2peak Module (Version 1.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoShenzhen Harveymed Technology Co., Ltd. — V series portable oxygen concentrator (V5, V5C, V6, V6C) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoVarian Medical Systems, Inc. — IDENTIFY (5.0) (510k cleared)MERIT MEDICAL SYSTEMS INC

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoCompanion Spine France — Companion Spine DIAM™ Instrumentation (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device 510k243d agoPolyConversions, Inc. — VR® Personal Protective Level 3 Gown (VR Gowns) (510k cleared)

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

    full page →fda device 510k ↗
    ›Dec 16, 2025device pma243d agoBard Peripheral Vascular, Inc. — LifeStent® Vascular Stent Systems (PMA supplement)

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

    full page →fda device pma ↗
    ›Dec 16, 2025device pma243d agoBausch & Lomb — Boston Orthokeratology (oprifocon A) (PMA supplement)Bausch & Lomb Corp

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

    full page →fda device pma ↗
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    $SNGX
    $ISRG394.51-1.68%
    $CODX1.51000.00%
    $PFE26.79-0.04%
    $ICUI182.98-0.07%
    $ICUI182.98-0.07%
    $BLCO17.05+0.41%
    $MMSI90.76+0.29%