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calendar

21,639 catalysts · 4,728 grant · 4,110 device 510k · 3,118 approval · 3,045 8k filing · 2,000 device pma · 2,000 device recall

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2026-08-10: 0 catalysts2026-08-11: 16 catalysts2026-08-12: 19 catalysts2026-08-13: 19 catalysts2026-08-14: 4 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 1 catalyst2026-08-18: 2 catalysts2026-08-19: 2 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: 8 catalysts2026-11-03: 17 catalysts2026-11-04: 22 catalysts2026-11-05: 36 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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type
  • grant4,728
  • device 510k4,110
  • approval3,118
  • 8k filing3,045
  • device pma2,000
  • device recall2,000
  • device adverse event1,000
  • recall973
  • earnings579
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Dec 30, 2024

    24
    ›Jan 2, 2025device 510k586d agoJiangxi Zhuoruihua Medical Instrument Co., Ltd. — Haemostasis Clips (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoEzra Ai, Inc. — Ezra Flash (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoGreenMark Biomedical, Inc. — CrystLCare™ PRO Biorestorative, Fluoride-Plus (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoBionit Labs Srl — Wave Electrode (AE02-60); Wave Electrode (AE02-50) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoMicro Therapeutics, Inc. d/b/a ev3 Neurovascular — Rist 079 Radial Access Guide Catheter; Rist 071 Radial Access Guide Catheter; Rist Radial Access Selective Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoOrtho Ai, LLC — Ortho AI (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoHunan Accurate Bio-Medical Technology Co., Ltd. — Pulse Oximeter (FS20P); Pulse Oximeter (FS20C); Pulse Oximeter (FS10C) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoDongguan Laiguang Electronic Technology Co., Ltd. — Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 2, 2025device 510k586d agoAnhui Jbh Medical Apparatus Co., Ltd. — Power Wheelchair (D03, D05, D06, D09, D11, D16, D22, D23, D26, D36) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025approval585d agoPYRUKYND (MITAPIVAT SULFATE) — FDA approvalAGIOS PHARMACEUTICALS, INC.

    Sponsor: AGIOS PHARMS INC. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Jan 3, 2025device 510k585d agoPentax of America, Inc. — PENTAX Medical Video Colonoscope (EC38-i20cWL) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoInbella Medical, Inc. — Inbella RF System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoEunsung Global Corp — DUET-V (Model: ESK-3261DV) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoProimtech Saglik Urunleri Anonim Sirketi — GBR System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoDk Medical System — INNOVISION-EXII (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoSiemens Medical Solutions USA, Inc. — syngo.CT Dual Energy (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoAbbott Point of Care, Inc. — i-STAT hs-TnI cartridge with the i-STAT 1 System (510k cleared)

    Product code: MMI. Advisory committee: Clinical Chemistry. Type: Traditional

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoInventis S.R.L. — Synapsys VHIT (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoMallinckrodt Manufacturing, LLC — EVOLVE Nitric Oxide Delivery System (510k cleared)Mallinckrodt LLC

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoNobel Biocare AB — NobelProcera Zirconia Implant Bridge (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoZinkh NV — Elemental Granulate (510k cleared)

    Product code: OLR. Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoOrmco Corporation — Ormco™ EtchFree Bonding System, Ormco™ EtchFree Bonding Primer, Ormco™ EtchFree Adhesive (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoGe Medical Systems Israel, Functional Imaging — Clarify DL (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 3, 2025device 510k585d agoJLK, Inc. — JLK-ICH (510k cleared)

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

    full page →fda device 510k ↗

    Week of Jan 6, 2025

    26
    ›Jan 6, 2025device 510k582d agoArum Dentistry Co., Ltd. — SD TL Implant System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k
    ← prev
    page 1 of 433
    next →
    582d ago
    United Orthopedic Corporation — Conformity Stem Extension Line, #0 (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k582d agoTHINK Surgical, Inc. — TMINI Miniature Robotic System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k582d agoShenzhen Sontu Medical Imaging Equipment Co., Ltd. — Digital Radiography X-ray System (SONTU100-RAD (E) , SONTU300-Mars (E)) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k582d agoYongkang Yile Vehicle Co., Ltd. — Mobility Scooter (YL-09B, YL-07) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k582d agoOmega Medical Imaging, LLC — Soteria E-View (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k582d agoBrainomix Limited — Brainomix 360 e-CTA (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k582d agoWhill, Inc. — WHILL Model R (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 6, 2025device 510k582d agoFesariustherapeutics, Inc. — DermiSphere Dermal Template (510k cleared)

    Product code: KGN. Advisory committee: Unknown. Type: Traditional

    full page →fda device 510k ↗
    ›Jan 7, 2025approval581d agoGABAPENTIN — FDA approvalGABAPENTIN

    Sponsor: ACTAVIS ELIZABETH. Form: CAPSULE. Route: ORAL

    full page →GABAPENTIN →fda approvals ↗
    ›Jan 7, 2025approval581d agoGABAPENTIN — FDA approvalGABAPENTIN

    Sponsor: ACTAVIS ELIZABETH. Form: CAPSULE. Route: ORAL

    full page →GABAPENTIN →fda approvals ↗
    ›Jan 7, 2025approval581d agoDEMEROL (MEPERIDINE HYDROCHLORIDE) — FDA approvalMEPERIDINE HYDROCHLORIDE

    Sponsor: HOSPIRA. Form: INJECTABLE. Route: INJECTION

    full page →MEPERIDINE HYDROCHLORIDE →fda approvals ↗
    ›Jan 7, 2025device 510k581d agoShanghai United Imaging Healthcare Co., Ltd. — uCT 780 (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 7, 2025device 510k581d agoCanon Medical Systems Corporation — Vantage Galan 3T, MRT-3020, V10.0 with AiCE Reconstruction Processing Unit for MR (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 7, 2025device 510k581d agoDRGEM Corporation — GXR-Series Diagnostic X-Ray System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 7, 2025device 510k581d agoAstura Medical — MASADA Modular Spinal Fixation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 7, 2025device 510k581d agoOrbusNeich Medical (Shenzhen) Co., Ltd. — COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 7, 2025device 510k581d agoTargeted Genomics, LLC — GlutenID Celiac Genetic Health Risk Test (510k cleared)Dawn Sea Therapeutics

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

    full page →fda device 510k ↗
    ›Jan 7, 2025device 510k581d agoCorin U.S.A. Limited — ApolloHipX (THR.SS.0001) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jan 8, 2025approval580d agoLAMOTRIGINE — FDA approvalZydus Therapeutics Inc

    Sponsor: ZYDUS PHARMS. Form: TABLET, EXTENDED RELEASE. Route: ORAL

    full page →fda approvals ↗
    ›Jan 8, 2025recall580d agoAvKARE recall (Cls III)AvKare LLC

    Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% Moisturizing Lubricant Eye Drops, 0.5 FL OZ (15 mL) bottles, Distributed by: AvKARE, Pulaski, TN, 38478, NDC 50268-068-15. — Reason: LABELING: LABEL MIX-UP — Status: Ongoing

    full page →fda recalls ↗
    ›Jan 8, 2025recall580d agoVIONA PHARMACEUTICALS INC recall (Cls II)IONIS PHARMACEUTICALS INC

    Dapsone Gel 7.5%, 90 g, Rx Only, Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India, Distributed by: Viona Pharmaceuticals Inc., Cranford, NJ 07016, NDC 72578-094-03. packaged in an Airless pump pack — Reason: Crystallization — Status: Ongoing

    full page →fda recalls ↗
    ›Jan 8, 2025recall580d agoAvKARE recall (Cls II)AvKare LLC

    Nitrofurantoin Capsules, USP, 100 mg, 50 Capsules (5 x 10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478. NDC#: 50268-625-15. — Reason: Failed Dissolution Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Jan 8, 2025recall580d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

    Levothyroxine Sodium Tablets, Lupin, 75 mcg (0.075mg), 1000 Tablets, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited, Pithampur (M.P)- 454 775 INDIA, NDC# 68180-967-03 — Reason: Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study. — Status: Terminated

    full page →fda recalls ↗
    ›Jan 8, 2025recall580d agoHikma Injectables USA Inc recall (Cls II)NRX Pharmaceuticals, Inc.

    ketamine inj 50 mg per 1 mL, Rx Only, 1 mL fill in a 3mL pre-filled syringe, For IV or IM Use, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, This is a Compounded Drug. Hospital/Office Use Only. NDC 63037-137-25 — Reason: Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment. — Status: Terminated

    full page →fda recalls ↗
    ›Jan 8, 2025recall580d agoGNMart LLC recall (Cls I)OCULAR THERAPEUTIX, INC

    FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles — Reason: Marketed without an approved NDA/ANDA. FDA analysis found the product to be tainted with Diclofenac and Dexamethasone. — Status: Ongoing

    full page →fda recalls ↗
    $AGIO32.59+0.99%
    $IONS56.94+0.67%
    $OCUL9.2400+0.54%
    $NRXP
    $LBRX45.85-4.48%