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calendar

20,183 catalysts · 4,728 grant · 3,189 8k filing · 3,076 device 510k · 2,774 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • 8k filing3,189
  • device 510k3,076
  • approval2,774
  • device pma2,000
  • device recall2,000
  • device adverse event1,000
  • recall751
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jun 9, 2025

    50
    ›Jun 11, 2025recall428d agoTorrent Pharma Inc. recall (Cls II)Torrent Pharma Inc

    Fluoxetine Tablets, USP, 20 mg, 28-count Carton (4x7 Unit-dose), Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-91 (Carton); 13668-473-70 (Blister) — Reason: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Jun 11, 2025recall428d agoAmerisource Health Services LLC recall (Cls II)ACP Nimble Buyer Inc

    Indomethacin Extended-Release Capsules, USP, 75 mg, 30 capsules (3 x 10 blister cards) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, NDC 68084-411-21 (carton), NDC 68084-411-11 (blister card). — Reason: cGMP deviations — Status: Ongoing

    full page →fda recalls ↗
    ›Jun 11, 2025recall428d agoConsumer Product Partners, LLC recall (Cls II)

    Spectrum Advanced Gel Hand Sanitizer, Ethyl alcohol 70%, 8 FL OZ (236 mL) per bottle, Manufactured for Medline Industries, Inc., Three Lakes Drive, Northfield, IL 60693 USA. NDC: 53329-202-08, UPC 8 88277 34945 5 — Reason: Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol — Status: Ongoing

    full page →fda recalls ↗
    ›Jun 11, 2025recall428d agoTorrent Pharma Inc. recall (Cls II)Torrent Pharma Inc

    Fluoxetine Tablets, USP, 20 mg, 30-count bottle, Rx only, Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-30 — Reason: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Jun 11, 2025recall428d agoApotex Corp. recall (Cls II)Apotex Corp

    Lacosamide Oral Solution, USP, 10 mg/mL, 200 mL, Rx Only, Manufactured by: Apotex Inc., Toronto, Ontario, Canada M9L 1T9, Manufactured for: Apotex Corp., Weston FL 33326, NDC 60505-0405-4 — Reason: Defective Container: This recall is being initiated due to a leaking unit stored horizontally. — Status: Ongoing

    full page →fda recalls ↗
    ›Jun 11, 2025device pma428d agoW. L. Gore & Associates, Inc. — GORE TAG Thoracic Branch Endoprosthesis (TBE Device) (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 11, 2025device pma428d agoVentana Medical Systems, Inc. — PATHWAY Anti-HER-2/neu (4B5) Rabbit Monoclonal Primary Antibody (PMA supplement)MERIT MEDICAL SYSTEMS INC

    Supplement type: Normal 180 Day Track. Product code: MVC. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Jun 11, 2025device pma428d agoW. L. Gore & Associates, Inc. — GORE® EXCLUDER® AAA Endoprosthesis (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 11, 2025device pma428d agoRxsight, Inc. — Light Adjustable Lens, Light Delivery System (PMA supplement)RxSight, Inc.

    Supplement type: Real-Time Process. Product code: PZK. Advisory committee: OP. Decision: APPR

    full page →fda device pma ↗
    ›Jun 11, 2025device pma428d agoLeMaitre Vascular, Inc. — Artegraft Collagen Vascular Graft (PMA supplement)LEMAITRE VASCULAR INC

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

    full page →fda device pma ↗
    ›Jun 11, 2025device 510k428d agoIntuitive Surgical, Inc. — da Vinci X Surgical System (IS4200); da Vinci Xi Surgical System (IS4000) (510k cleared)INTUITIVE SURGICAL INC

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoNvision Biomedical Technologies — Impact PEEK Union Nail System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoBoston Scientific Corporation — Rezum System (510k cleared)BOSTON SCIENTIFIC CORP

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoBonebridge AG — LORRAINE 2.5/3.5mm Distal Humerus System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoMedtronic, Ireland — Liberant Thrombectomy System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoWilliam Cook Europe Aps — Frova Intubating Introducer (C-CAE-14.0-70-FII); Frova Intubating Introducer (C-CAE-14.0-70-FI); Frova Intubating Introducer (C-CAE-14.0-70-FIC); Frova Intubating Introducer (C-CAE-14.0-70-FIC-SPOPS) (510k cleared)

    Product code: BTR. Advisory committee: Anesthesiology. Type: Special

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoGI Windows, Inc. — Self-Forming Magnet (Flexagon) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoAmbu A/S — Ambu® aScope™ 5 Cysto HD (Standard Deflection); Ambu® aScope™ 5 Cysto HD (Reverse Deflection) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoCarl Zeiss Meditec Cataract Technology, Inc. — MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 11, 2025device 510k428d agoEnpuno Co., Ltd. — Injectable Root Canal Bioceramic Sealer (nRoot SP) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025approval427d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

    Sponsor: MERCK SHARP DOHME. Form: SOLUTION. Route: INTRAVENOUS

    full page →pembrolizumab →fda approvals ↗
    ›Jun 12, 2025approval427d agoVOQUEZNA TRIPLE PAK (AMOXICILLIN) — FDA approvalamoxicillin + clarithromycin + vonoprazan

    Sponsor: PHATHOM. Form: CAPSULE, TABLET, TABLET. Route: ORAL

    full page →amoxicillin + clarithromycin + vonoprazan →fda approvals ↗
    ›Jun 12, 2025approval427d agoVOQUEZNA DUAL PAK (AMOXICILLIN) — FDA approvalamoxicillin + vonoprazan fumarate

    Sponsor: PHATHOM. Form: CAPSULE, TABLET. Route: ORAL

    full page →amoxicillin + vonoprazan fumarate →fda approvals ↗
    ›Jun 12, 2025approval427d agoDELSTRIGO (DORAVIRINE) — FDA approval(doravirine + lamivudine + tenofovir disoproxil fumarate)

    Sponsor: MSD MERCK CO. Form: TABLET. Route: ORAL

    full page →(doravirine + lamivudine + tenofovir disoproxil fumarate) →fda approvals ↗
    ›Jun 12, 2025device pma427d agoBiotronik, Inc. — Sentus QP Pacing Leads (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: NKE. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Jun 12, 2025device pma427d agoMedtronic, Inc. — Harmony Transcatheter Pulmonary Valve System (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Jun 12, 2025device pma427d agoBiotronik, Inc. — Sentus QP Pacing Leads (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: MRM. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Jun 12, 2025device pma427d agoEndotronix, Inc. — Cordella Pulmonary Artery Sensor System (CorPASS) (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 12, 2025device pma427d agoMedtronic Vascular — Endurant Stent Graft System (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 12, 2025device pma427d agoRayner Intraocular Lenses , Ltd. — C-flex lntraocular Lens; C-flex Aspheric lntraocular Lens; 6.0 mm Aspheric lntraocular Lens; RayOne Aspheric; RayOne Sph (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 12, 2025device pma427d agoMedtronic Vascular — Valiant Thoracic Stent Graft with the Captivia Delivery System (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 12, 2025device 510k427d agoHt Medical D.B.A. Xenix Medical — RIVA Posterior Fixation System; RIVA Posterior Fixation System Navigation Instruments (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoNovapproach Spine, LLC — OneLIF™ Interbody Fusion System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoBiomérieux — ETEST Aztreonam/Avibactam (AZA) (0.016/4-256/4 µg/mL) (510k cleared)Bristol-Myers Squibb Co

    Product code: JWY. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoDavol, Inc. — Bard® Mesh; Bard® Mesh Pre-Shaped (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoZhengzhou PZ Laser Slim Technology Co., Ltd. — Fractional CO2 Laser Machine (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoSmith & Nephew, Inc. — TRIGEN Stable Lock Nut & Washer (510k cleared)SMITH & NEPHEW PLC

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoGe Medical Systems Israel — Aurora (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoEl.En S.P.A. — Deka Bluebeam (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoId-Fish Technology, Inc. — iDart Lyme IgM ImmunoBlot Kit (510k cleared)Fort Technology Inc

    Product code: LSR. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoBiocomposites, Ltd. — Synicem Hip Spacer; Synicem Knee Spacer; Synicem Shoulder Spacer (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoBeijing Sano Laser S&T Development Co.,Ltd — Q-Switched Nd:YAG Laser (SHE-LSP101-1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoJeil Medical Corporation — FIX-L PEEK PLIF and T-PLIF System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoGm Dos Reis Industria E Comercio — GMReis Fibula Nail System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoLg Electronics.Inc — Medical Monitor (32HS710S) (510k cleared)ARROW ELECTRONICS, INC.

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoPearl, Inc. — Second Opinion® CS (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoMedtronic Sofamor Danek, Inc. — Grafton™ DBM; Grafton Plus™ DBM Paste; Magnifuse™ Bone Graft (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoDmax Co., Ltd. — Multi M Series (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoOlympus Medical Systems Corporation — Disposable Cytology Brush BC-202D/203D Series (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 12, 2025device 510k427d agoThermo Fisher Scientific (Oxoid Ltd.) — Thermo Scientific Oxoid Aztreonam/Avibactam Disc (30/20 µg) AZA50 (510k cleared)THERMO FISHER SCIENTIFIC INC.

    Product code: JTN. Advisory committee: Microbiology. Type: Traditional

    full page →fda device 510k ↗
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    $LMAT82.13-0.86%
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    $RXST
    $PHAT9.1700+7.76%
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    $BSX51.55+0.70%
    $SNN29.88-0.45%
    $PHAT9.1700+7.76%
    $FRTT
    $MDT90.76+0.09%
    $MRK132.92+1.92%
    $TMO447.81+1.31%
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