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14,311 catalysts · 3,393 8k filing · 2,402 grant · 2,350 approval · 1,681 device 510k · 1,204 device recall · 1,151 device pma

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  • 8k filing3,393
  • grant2,402
  • approval2,350
  • device 510k1,681
  • device recall1,204
  • device pma1,151
device adverse event
1,000
  • earnings584
  • recall465
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Nov 24, 2025

    50
    ›Nov 25, 2025approval267d agoSCEMBLIX (ASCIMINIB HYDROCHLORIDE) — FDA approvalasciminib hydrochloride

    Sponsor: NOVARTIS. Form: TABLET. Route: ORAL

    full page →asciminib hydrochloride →fda approvals ↗
    ›Nov 25, 2025approval267d agoVOYXACT (SIBEPRENLIMAB-SZSI) — FDA approvalsibeprenlimab

    Sponsor: OTSUKA PHARM CO LTD. Form: INJECTABLE. Route: INJECTION

    full page →sibeprenlimab →fda approvals ↗
    ›Nov 25, 2025approval267d agoIMFINZI (DURVALUMAB) — FDA approvalASTRAZENECA PLC

    Sponsor: ASTRAZENECA UK LTD. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval267d agoACETAZOLAMIDE — FDA approvalAccord Healthcare Inc

    Sponsor: HIBROW HLTHCARE. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval267d agoCHILDREN'S CETIRIZINE HYDROCHLORIDE HIVES RELIEF (CETIRIZINE HYDROCHLORIDE) — FDA approvalKenvue Inc.

    Sponsor: BAJAJ. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval267d agoPERAMPANEL — FDA approvalCATALYST PHARMACEUTICALS, INC.

    Sponsor: TARO. Form: TABLET. Route: ORAL

    full page →fda approvals ↗
    ›Nov 25, 2025approval267d agoNOREPINEPHRINE BITARTRATE — FDA approvalBaxter Healthcare Corp

    Sponsor: ANTHEA PHARMA. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Nov 25, 2025approval267d agoIRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE) — FDA approvalALDACTAZIDE

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

    full page →ALDACTAZIDE →fda approvals ↗
    ›Nov 25, 2025approval267d agoPERAMPANEL — FDA approvalPERAMPANEL

    Sponsor: MSN. Form: TABLET. Route: ORAL

    full page →PERAMPANEL →fda approvals ↗
    ›Nov 25, 2025device 510k267d agoOlympus Medical Systems Corporation — Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoIndica Labs, LLC — HALO AP Dx (510k cleared)

    Product code: QKQ. Advisory committee: Pathology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoEncore Guards — enCore Night Guard (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoStemtech Medical Devices Private Limited — Eva Scalp Cooling System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoAkura Medical — Akura Thrombectomy System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoGood Sleep CO Pte , Ltd. — Hushd Avera (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoUzinmedicare Co., Ltd. — Spectra Platinum (510k cleared)

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoTrustees of the University of Pennsylvania — PennPET Explorer Positron Emission Tomograph (510k cleared)University of Pennsylvania

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoShenzhen Leaflife Technology Co., Ltd. — LeafPure-Echo (LM-LPNdA) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoRay Co., Ltd. — RCT700 (510k cleared)Ray Therapeutics Inc

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoFeops NV — FEops HEARTguide Simulation Application (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoMedusa Orthopedics, LLC — Medusa Orthopedics Boa External Fixation System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoDongguan Lide Electric Appliance Co., Ltd. — IPL Hair Removal Device (KA-10, KA-11, KA-11C, KA-11D, KA-18, KA-20, KA-21, KA-21C) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoNaox Technologies Sas — NX01 (NX01) (510k cleared)Niu Technologies

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoGeistlich Pharma AG — Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide® (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoZsfab, Inc. — ZSFab Lumbar Interbody System (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoEsaote, S.p.A. — 7600 Ultrasound System (MyLabC25); 7600 Ultrasound System (MyLabC30) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoMlhealth 360 — Scaida BrainCT-ICH (v1.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoSpeclipse, Inc. — BELLUS-Q (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device 510k267d agoLuxCreo, Inc. — LuxCreo Flexible Partial Denture Resin (510k cleared)

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

    full page →fda device 510k ↗
    ›Nov 25, 2025device pma267d agoMicroPort CRM USA, Inc. — ENERGYA/TALENTIA ICDs & CRT-Ds, SmartTouch Programmer Software Modules, SmartView Connect App, & RMS (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoEndotronix, Inc. — CorPASS System (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoMicroPort CRM USA, Inc. — ENERGYA/TALENTIA ICDs & CRT-Ds, SmartTouch Programmer Software Modules, SmartView Connect App, & RMS (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoLivaNova USA, Inc. — VNS Therapy Model 3100 Programmer, VNS Therapy Model 2000 Programming Wand (PMA supplement)

    Supplement type: Real-Time Process. Product code: LYJ. Advisory committee: NE. Decision: APPR

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoMicroPort CRM USA, Inc. — ENERGYA/TALENTIA ICDs & CRT-Ds, SmartTouch Programmer Software Modules, SmartView Connect App, & RMS (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoMedtronic, Inc. — Micra Transcatheter Pacing Systems (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoInstylla, Inc. — Embrace(TM) Hydrogel Embolic System (PMA supplement)

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

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoXvivo Perfusion, Inc. — XPS™ with Steen Solution™ Perfusate (PMA supplement)

    Supplement type: Real-Time Process. Product code: PHO. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Nov 25, 2025device pma267d agoLumicell, Inc. — Lumicell Direct Visualization System (DVS) (PMA supplement)

    Supplement type: Special (Immediate Track). Product code: SAW. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Nov 25, 2025device recall267d agoFerndale Laboratories, Inc. device recall (Cls II)G&W Laboratories Inc

    Brand Name: Mastisol Liquid Adhesive Product Name: Liquid Adhesive Model/Catalog Number: 0523-48 Product Description: Liquid adhesive, 2/3 mL vial, 48 vials per carton Component: No — Reason: Butyrate tube cracks during actuation, rendering product unusable. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 25, 2025grant267d agoLAUREATE INSTITUTE FOR BRAIN RESEARCH — Mechanisms of Low-Intensity Focused Ultrasound Neuromodulation for Post-Traum...

    GM grant. $431,302. PI: Adrienne A Taren

    full page →nih reporter ↗
    ›Nov 26, 2025approval266d agoVALBENAZINE TOSYLATE — FDA approvalVALBENAZINE TOSYLATE

    Sponsor: ZYDUS LIFESCIENCES. Form: CAPSULE. Route: ORAL

    full page →VALBENAZINE TOSYLATE →fda approvals ↗
    ›Nov 26, 2025approval266d agoDALBAVANCIN HYDROCHLORIDE — FDA approvalFresenius Kabi USA LLC

    Sponsor: KINDOS. Form: POWDER. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Nov 26, 2025approval266d agoCABENUVA KIT (CABOTEGRAVIR) — FDA approvalViiV Healthcare Company

    Sponsor: VIIV HLTHCARE. Form: SUSPENSION, EXTENDED RELEASE. Route: INTRAMUSCULAR

    full page →fda approvals ↗
    ›Nov 26, 2025recall266d agoDermaRite Industries, LLC recall (Cls II)

    Lantiseptic, Skin Protectant, Lanolin USP 30%, packaged in a) 5g (0.17 oz) (NDC 61924-304-05), b)14.2g (0.5 oz)( NDC 61924-304-14), c) 4oz (NDC 61924-304-04), d) 4.5oz (NDC 61924-304-45), and e) 12oz (NDC 61924-304-12) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall266d agoDermaRite Industries, LLC recall (Cls II)

    KleenFoam Antimicrobial Foam Soap, Chloroxylenol 0.5%, 34 FL OZ (1000 mL) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-093-34 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall266d agoDermaRite Industries, LLC recall (Cls II)Insight Pharmaceuticals LLC

    DermaFungal, Antifungal Cream with 2% Miconazole Nitrate, packaged in a) 5 g (0.18 oz) per packet (NDC 61924-234-05), and b)106 g (3.75 oz.) per tube (NDC 61924-234-04) DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall266d agoDermaRite Industries, LLC recall (Cls II)

    DermaSarra, Camphor 0.5%, External Analgesic, 222 mL (7.5 fl. oz.) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-189-08 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall266d agoDermaRite Industries, LLC recall (Cls II)

    PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-198-08 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall266d agoDermaRite Industries, LLC recall (Cls II)

    DermaMed Ointment, Skin Protectant, Aluminum Hydroxide Gel 2%, Net Wt. 106 g (3.75 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-214-04 — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
    ›Nov 26, 2025recall266d agoDermaRite Industries, LLC recall (Cls II)

    PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC 61924-205-07) tubes, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. — Reason: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated. — Status: Ongoing

    full page →fda recalls ↗
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