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8,918 catalysts · 3,315 8k filing · 1,702 grant · 1,000 device adverse event · 795 approval · 621 device 510k · 584 earnings

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2026-08-10: 0 catalysts2026-08-11: 0 catalysts2026-08-12: 0 catalysts2026-08-13: 0 catalysts2026-08-14: 31 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 3 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 1 catalyst2026-08-27: 1 catalyst2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 1 catalyst2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 2 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 2 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 1 catalyst2026-10-14: 1 catalyst2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 1 catalyst2026-10-20: 2 catalysts2026-10-21: 2 catalysts2026-10-22: 2 catalysts2026-10-23: 1 catalyst2026-10-24: 0 catalysts2026-10-25: 0 catalysts2026-10-26: 1 catalyst2026-10-27: 8 catalysts2026-10-28: 12 catalysts2026-10-29: 21 catalysts2026-10-30: 4 catalysts2026-10-31: 0 catalysts2026-11-01: 0 catalysts2026-11-02: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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  • 8k filing3,315
  • grant1,702
  • device adverse event1,000
  • approval795
  • device 510k621
  • earnings584
device pma
467
  • device recall191
  • phase 2 completion172
  • recall162
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Mar 2, 2026

    50
    ›Mar 3, 2026approval165d agoLETROZOLE — FDA approvalYiling Pharmaceutical Ltd

    Sponsor: PHARMOBEDIENT. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Mar 3, 2026approval165d agoTRACLEER (BOSENTAN) — FDA approvalJanssen-Cilag Holdings Inc (Inactive)

    Sponsor: ACTELION. Form: TABLET, FOR SUSPENSION. Route: ORAL

    full page →fda approvals ↗
    ›Mar 3, 2026device 510k165d agoZhejiang Hangkang Medical Equipment Co., Ltd. — Surgical Face Mask (Ear mount) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoL&K BIOMED Co., Ltd. — PathLoc Lumbar Plate System (510k cleared)NeuCen BioMed Co Ltd

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoRam.Shaw Pte. , Ltd. — Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoHarrison-AI Medical Pty, Ltd. — Annalise Enterprise (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoTHINK Surgical, Inc. — TMINI® Miniature Robotic System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoSota Cloud Corp. — SOTA Cloud Smart Sensor (1.5) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoHaidari Beauty Technology (Beijing) Co., Ltd. — CO2 Laser Treatment Machine (CFR3M1) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoArthrex, Inc. — Arthrex Humeral Plating System (Anatomic Humeral Plate) and Cerclage Button (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoNew Stetic, SA — ZAFIRA® (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoShenzhen Hanhua Opto Co., Ltd. — LED Therapy Light (COB1400, HP1800PRO) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device 510k165d agoPremier Dental Products Company — Bond-PR™ Universal Adhesive (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 3, 2026device pma165d agoMedtronic, Inc. — Mosaic Neo Mitral Bioprosthesis (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Mar 3, 2026device pma165d agoPerimeter Medical Imaging Ai, Inc. — Claire™ OCT System (PMA)

    Product code: SHH. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Mar 3, 2026device pma165d agoMedtronic, Inc. — HexaGen™ RF Generator (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Mar 3, 2026device pma165d agoValencia Technologies Corporation — eCoin Peripheral Neurostimulator (PMA supplement)

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

    full page →fda device pma ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/15 OR Table; System Code: 722059; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 5 M12; System Code: (1)722227, (2)722231; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoOxoid Australia Pty Limited device recall (Cls II)THERMO FISHER SCIENTIFIC INC.

    OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem — Reason: Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result from ambiguous color reactions in wells. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD10F; System Code: 722002; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/10; System Code: 722029; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD20 OR Table; System Code: (1) 722015, (2)722023, (3)722035; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 3 M15; System Code: (1)722064, (2)722222, (3)722230, (4)722280 (OUS Only); — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 5 M20; System Code: (1)722228, (2)722232, (3) 722281 (OUS only); — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/20 OR Table; System Code: 722039; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/15; System Code: 722058; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/20; System Code: 722038; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only); — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10C; System Code: 722001; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026device recall165d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026; — Reason: Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch. — Status: Ongoing

    full page →fda device recalls ↗
    ›Mar 3, 2026grant165d agoVANDERBILT UNIVERSITY — Transcranial Functional Ultrasound in Adult Humans

    EB grant. $542,947. PI: Brett C Byram

    full page →nih reporter ↗
    ›Mar 3, 2026grant165d agoUNIVERSITY OF MISSISSIPPI — Ionic liquid-assisted drug delivery to brain reservoirs for treatment of neur...

    DA grant. $101,214. PI: Jason Richard Paris

    full page →nih reporter ↗
    ›Mar 3, 2026grant165d agoGORDON RESEARCH CONFERENCES — 2026 Immunoengineering Gordon Research Conference and Gordon Research Seminar

    AI grant. $19,000. PI: Nicole Franziska Steinmetz

    full page →nih reporter ↗
    ›Mar 3, 2026grant165d agoKEYSTONE SYMPOSIA — RNA Modifications: Bridging Biological Function and Therapeutic Potential

    CA grant. $10,000. PI: TERRY L. SHEPPARD

    full page →nih reporter ↗
    ›Mar 3, 2026grant165d agoMAYO CLINIC ROCHESTER — Acute Kidney Injury in Care Transitions: The ACT Pragmatic TrialMayo Clinic

    DK grant. $796,370. PI: Erin Frazee Barreto

    full page →nih reporter ↗
    ›Mar 3, 2026grant165d agoKEYSTONE SYMPOSIA — Cancer Immunotherapy: Basic Mechanisms Informing Clinical Applications & Comb...

    CA grant. $5,000. PI: TERRY L. SHEPPARD

    full page →nih reporter ↗
    ›Mar 3, 2026grant165d agoMICHIGAN STATE UNIVERSITY — Probing nucleolus function in a mouse model of fragile X syndrome

    MH grant. $416,859. PI: Hongbing Wang

    full page →nih reporter ↗
    ›Mar 3, 2026grant165d agoUNIVERSITY OF CALIFORNIA, SAN DIEGO — Functional RNA elements in the human genomeUniversity of California San Diego

    HG grant. $785,329. PI: Kevin Daniel Corbett

    full page →nih reporter ↗
    ›Mar 4, 2026approval164d agoBAL (DIMERCAPROL) — FDA approvalAkorn Operating Company LLC (Inactive)

    Sponsor: PROVEPHARM SAS. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Mar 4, 2026approval164d agoROCURONIUM BROMIDE — FDA approvalROCURONIUM BROMIDE

    Sponsor: ASPIRO. Form: INJECTABLE. Route: INJECTION

    full page →ROCURONIUM BROMIDE →fda approvals ↗
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