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21,856 catalysts · 4,728 grant · 4,087 device 510k · 3,286 8k filing · 3,117 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k4,087
  • 8k filing3,286
  • approval3,117
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall973
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Feb 10, 2025

    50
    ›Feb 12, 2025recall548d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

    Carvedilol Tablets, USP, 12.5 mg, Rx only, a)500 Tablets, NDC 68462-164-05; b) 100 Tablets, NDC 68462-164-01, Manufactured for Glenmark Pharmaceuticals, NJ. — Reason: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025recall548d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

    Carvedilol Tablets, USP, 25 mg, Rx only, a)500 Tablets, NDC 68462-165-05; b) 100 Tablets, NDC 68462-165-01, Manufactured for Glenmark Pharmaceuticals, NJ. — Reason: CGMP Deviations:N-Nitroso Carvedilol I impurity (NNCI-I) were found to be failing per current FDA recommended limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025recall548d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Aurobindo Pharma USA Inc

    Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton (10 x 10 unit dose blisters), Rx Only, Distributed by: Aurobindo Pharma USA< INC., 279 Princeton-Hightstown Road, East Windsor, NJ 08520. Made in India. Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152. NDC: 0904-7216-61 — Reason: Failed Dissolution Specifications. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025recall548d agoTeva Pharmaceuticals USA, Inc recall (Cls II)Terns Pharmaceuticals, Inc.

    Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as a) 1 syringe in 1 CARTON, NDC 63459-910-11, Blister NDC 63459-910-12; (b)10 syringes in 1 CARTON, NDC 63459-910-15, Blister NDC 63459-910-12; (c) 1 syringe in 1 CARTON, NDC 63459-910-17 without safety guard and blister, Rx Only, Manufactured by: UAB Teva Baltics, Vilnius, Lithuania. Distributed by Teva Pharmaceuticals USA, Inc. North Wales PA 19454. Product of Israel. — Reason: Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025recall548d agoENDO USA, Inc. recall (Cls I)Par Pharmaceutical Inc

    Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 42023-103-01 — Reason: Labeling: Not Elsewhere Classified: misleading label similar in appearance to the FDA-approved drug product Adrenalin¿ (epinephrine injection, USP) — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025recall548d agoSKY PACKAGING recall (Cls II)Strides Pharma Science Ltd

    HydrALAZINE Hydrochloride, 100 Tablets (10x10), USP, 50mg, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-328-10 — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025recall548d agoSKY PACKAGING recall (Cls II)Strides Pharma Science Ltd

    HydrALAZINE Hydrochloride, 25 mg, 100 Unit Dose Tablets (10x10), USP, Rx only, Manufactured by Strides Pharma Science Ltd, Bengaluru, India, Distributed by McKesson by: McKesson Corporation dba SKY Packaging, TN 38141. NDC 63739-327-10 — Reason: Failed Impurities/Degradation Specifications — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025recall548d agoFDC Limited recall (Cls II)FDC Ltd

    Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles, Rx only, Manufactured by: FDC Limited, Waluj, Aurangabad, Maharashtra, India, Distributed by: Rising Pharmaceuticals Inc, New Jersey, NDC 64980-514-05. — Reason: Defective Container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 12, 2025device 510k548d agoKunshan Hi-Fortune Health Products Co., Ltd. — Electrically Powered Wheelchair (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoAspen Imaging Healthcare, Inc. — AspenView (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoKunshan Hi-Fortune Health Products Co., Ltd. — Electrically Powered Wheelchair (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoOpsens, Inc. — OptoMonitor 3 (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoSiemens Medical Solutions USA, Inc. — NAEOTOM Alpha.Peak/ NAEOTOM Alpha; NAEOTOM Alpha.Pro; NAEOTOM Alpha.Prime (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoSamsung Medison Co., Ltd. — V8 Diagnostic Ultrasound System; cV8 Diagnostic Ultrasound System; V7 Diagnostic Ultrasound System; cV7 Diagnostic Ultrasound System; V6 Diagnostic Ultrasound System; cV6 Diagnostic Ultrasound System (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoGi Bionics, LLC — Fecobionics Anorectal System (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoSubtle Medical, Inc. — SubtleHD (1.x) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoQuality Electrodynamics, LLC — SureWave Elastography (Q7000225) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoEtiometry, Inc. — Etiometry Platform (DAV 5.4 RAE 9.2) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoBiokit, S.A. — ARCHITECT HSV-2 IgG, ARCHITECT HSV-2 IgG Calibrator, ARCHITECT HSV-2 IgG Controls (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 12, 2025device 510k548d agoZimmer, Inc. — Affixus Tibial Nailing System - 4mm screws (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025approval547d agoTRUQAP (CAPIVASERTIB) — FDA approvalcapivasertib

    Sponsor: ASTRAZENECA. Form: TABLET. Route: ORAL

    full page →capivasertib →fda approvals ↗
    ›Feb 13, 2025approval547d agoDENOSUMAB-DSSB — FDA approvaldenosumab biosimilar

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →denosumab biosimilar →fda approvals ↗
    ›Feb 13, 2025device 510k547d agoMaxx Orthopedics, Inc. — Freedom® Total Knee System - Porous Tibial Base Plate (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoAssure Tech., LLC — FaStep Pregnancy Rapid Test Cassette; Fastep HCG Rapid Test Cassette (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoNewclip Technics — Newclip Patient-matched instrumentation non sterile PSI (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoDentsply Sirona, Inc. — AH Plus Endodontic Sealer (510k cleared)DENTSPLY SIRONA Inc.

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoPenumbra, Inc. — Penumbra System (Reperfusion Catheter RED 72) (510k cleared)Penumbra Inc

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoHologic, Inc. — Aptima SARS-CoV-2 Assay (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoBoston Aesthetics, Inc. — Unicorn+ RF System (Unicorn+); Unicorn+ RF System (Unicorn+ I); Unicorn+ RF System (Unicorn+ II); Unicorn+ RF System (Unicorn+ III) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoJmt Co., Ltd. — EDEN ControlCath (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoNeuromodulatory Devices & Applications — Ampa One System (AMPA-001) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoDenjoy Dental Co., Ltd. — Integrated Endo System (Meet Endo-II) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 13, 2025device 510k547d agoFitbit, LLC — Body Temperature Software (BTS) (510k cleared)

    Product code: QZA. Advisory committee: General Hospital. Type: Special

    full page →fda device 510k ↗
    ›Feb 14, 2025approval546d agoROMVIMZA (VIMSELTINIB) — FDA approvalDeciphera Pharmaceuticals Inc

    Sponsor: DECIPHERA PHARMS. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Feb 14, 2025approval546d agoRYBREVANT (AMIVANTAMAB-VMJW) — FDA approvalamivantamab

    Sponsor: JANSSEN BIOTECH. Form: INJECTABLE. Route: INJECTION

    full page →amivantamab →fda approvals ↗
    ›Feb 14, 2025approval546d agoSIMLANDI (ADALIMUMAB-RYVK) — FDA approvalAlvotech

    Sponsor: ALVOTECH USA INC. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Feb 14, 2025device 510k546d agoAbbott Molecular, Inc. — Alinity m Resp-4-Plex (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoCoreline Soft Co., Ltd. — AVIEW CAC (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoShenzhen Kaiyan Medical Equipment Co., Ltd. — CurrentBody™ LED 4 in 1 Zone Facial Mapping Mask (MK-90C, MK-90M, MK66RB-F, MK-90N) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoLimFlow, Inc. — LimFlow V-Ceiver (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoAidoc Medical , Ltd. — BriefCase-Triage (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoTerrats Medical SL — DESS Dental Smart Solutions (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoNew World Medical, Inc. — VIA360™ Surgical System (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoWontech Co., Ltd. — WONTECH Surgical Optic Fibers (BA400/BA400R/BA600/BA600R) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoWontech Co., Ltd. — Pastelle Pro (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoWard 24/7 Aps — WARD-CSS (v1.2.x) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoShenzhen Finicare Co., Ltd. — Non-contact Forehead Infrared Thermometer (FC-IR2000, FC-IR205, FC-IR202, FC-IR206, FC-IR207, FC-IR209) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoBrainomix Limited — Brainomix 360 e-ASPECTS (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoVATECH Co., Ltd. — Green X 21 (PHT-90CHO) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 14, 2025device 510k546d agoNatus Medical Denmark Aps — ICS Dizcovery (1091) (510k cleared)

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

    full page →fda device 510k ↗
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