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21,138 catalysts · 4,728 grant · 3,704 device 510k · 3,111 8k filing · 3,015 approval · 2,000 device pma · 2,000 device recall

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  • grant4,728
  • device 510k3,704
  • 8k filing3,111
  • approval3,015
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall915
  • earnings583
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Feb 24, 2025

    50
    ›Feb 26, 2025recall532d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

    Atomoxetine Capsules, USP, 40 mg, 30 capsule bottles, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., NJ, USA, Product of India, NDC 68462-268-30. — Reason: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 26, 2025recall532d agoThe Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories recall (Cls II)Leading Pharma LLC

    Lorazepam Tablets, USP, 2mg, Unit Dose, 100 tablets per carton (10 x 10 blister packs), Rx only, The drug product contained in this package is from NDC # 69315-906 Leading Pharma, LLC., Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 26268 USA, NDC: 0904-6009-61. — Reason: Failed impurities/degradation specifications and Sub-potent Drug: Out-of-specification results were obtained during routine stability testing for Assay and Impurities. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 26, 2025recall532d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

    Atomoxetine Capsules, USP, 10 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Glenmark Pharmaceuticals Ltd., Goa, India, NDC 16714-755-01. — Reason: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 26, 2025recall532d agoGlenmark Pharmaceuticals Inc., USA recall (Cls II)LB PHARMACEUTICALS INC

    Atomoxetine Capsules, USP, 40 mg, 30 capsule bottles, Rx Only, Manufactured for: Northstar Rx LLC., Memphis, TN 38141, Manufactured by: Glenmark Pharmaceuticals Ltd., Goa, India, NDC 16714-758-01. — Reason: CGMP Deviations: presence of N-Nitroso Atomoxetine Impurity above the FDA recommended limit. — Status: Ongoing

    full page →fda recalls ↗
    ›Feb 26, 2025device 510k532d agoInfraredx, Inc. — Makoto Intravascular Imaging System™ (VC-MC10 / TVC-MC10i); Dualpro™ IVUS+NIRS Imaging Catheter (TVC-C195-42); Peripheral 014 Imaging Catheter (TVC-E195-42 ) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoInquis Medical — Aventus Thrombectomy System (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoPerfuze, Ltd. — Millipede 070 Aspiration Catheter; Perfuze Aspiration Tube Set (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoEl.En S.P.A. — DEKA LOTUS (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoSteriLance Medical (Suzhou), Inc. — Disposable Blood Lancet (Soft Pro); Disposable Blood Lancet (Softsure); Disposable Blood Lancet (Softsure Pro); Disposable Blood Lancet (Softsense) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoSteriLance Medical (Suzhou), Inc. — Heel Incision Safety Lancet (SteriHeel 2) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoVygon Corporation — pilot TLS (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoVentripoint Diagnostics , Ltd. — Ventripoint Medical System Plus (VMS+) 4.0 (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoElute, Inc. — BonVie+ (510k cleared)ELUTIA INC.

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoMedline Industries, LP — Medline Level 4 Surgical Gown with Breathable Sleeves (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoFovia, Inc. — aiCockpit AI Viewer (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 26, 2025device 510k532d agoMaquet Cardiovascular, LLC — Vasoview Hemopro 3 Power Supply (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 27, 2025approval531d agoPADCEV (ENFORTUMAB VEDOTIN-EJFV) — FDA approvalenfortumab vedotin

    Sponsor: ASTELLAS. Form: INJECTABLE. Route: INJECTION

    full page →enfortumab vedotin →fda approvals ↗
    ›Feb 27, 2025device 510k531d agoNanofiber Solutions, LLC — Rotium (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoVeol Medical Technologies Pvt , Ltd. — EzVu Visual Vasopressor injector (EV-19) (510k cleared)KESTRA MEDICAL TECHNOLOGIES, LTD.

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoXod, Inc. — XOD Diathermia Radiofrequency Device (510k cleared)Xos, Inc.

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoGleamer Sas — ChestView US (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoVascutek, Ltd. — Gelweave™ Vascular Prostheses (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoIline Microsystems, S.L. — microINR System (510k cleared)

    Product code: GJS. Advisory committee: Hematology. Type: Traditional

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoIcotec AG — VADER® Pedicle System and VADER®one Pedicle System (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoHangzhou AllTest Biotech Co., Ltd. — AllTest Multi-Drug Rapid Test Cup ; AllTest Multi-Drug Test Cup (510k cleared)Hangzhou DAC Biotech Co Ltd

    Product code: NFT. Advisory committee: Clinical Toxicology. Type: Traditional

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoXaga Surgical — Forsvall biopsy needle system for prostate biopsy (Forsvall biopsy gun and Forsvall biopsy needle) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoBecton Dickinson Infusion Therapy Systems, Inc. — PIVO™ Pro Needle-free Blood Collection Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoThermo Fisher Scientific — The Sensititre YeastOne Susceptibility System with Micafungin in the dilution range of 0.008-16 µg/mL (510k cleared)THERMO FISHER SCIENTIFIC INC.

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoL&K BIOMED Co., Ltd. — CastleLoc Pectus Bar System (510k cleared)NeuCen BioMed Co Ltd

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

    full page →fda device 510k ↗
    ›Feb 27, 2025device 510k531d agoBrosmed Medical Co., Ltd. — Parafleet SC 014 PTA Balloon Dilatation Catheter; Parafleet SC 018 PTA Balloon Dilatation Catheter; Parafleet SC 035 PTA Balloon Dilatation Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 28, 2025approval530d agoONTRUZANT (TRASTUZUMAB-DTTB) — FDA approvalONTRUZANT

    Sponsor: SAMSUNG BIOEPIS CO LTD. Form: POWDER. Route: IV (INFUSION)

    full page →ONTRUZANT →fda approvals ↗
    ›Feb 28, 2025approval530d agoAK-FLUOR 25% (FLUORESCEIN SODIUM) — FDA approvalLong Grove Pharmaceuticals LLC

    Sponsor: LONG GROVE PHARMS. Form: INJECTABLE. Route: INTRAVENOUS

    full page →fda approvals ↗
    ›Feb 28, 2025approval530d agoLYBALVI (OLANZAPINE) — FDA approval(olanzapine + samidorphan l-malate)

    Sponsor: ALKERMES INC. Form: TABLET. Route: ORAL

    full page →(olanzapine + samidorphan l-malate) →fda approvals ↗
    ›Feb 28, 2025approval530d agoZILBRYSQ (ZILUCOPLAN SODIUM) — FDA approvalzilucoplan

    Sponsor: UCB INC. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →zilucoplan →fda approvals ↗
    ›Feb 28, 2025approval530d agoZILBRYSQ (ZILUCOPLAN SODIUM) — FDA approvalzilucoplan

    Sponsor: UCB INC. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →zilucoplan →fda approvals ↗
    ›Feb 28, 2025approval530d agoTYENNE (TOCILIZUMAB-AAZG) — FDA approvalTYENNE

    Sponsor: FRESENIUS KABI USA. Form: INJECTABLE. Route: INTRAVENOUS

    full page →TYENNE →fda approvals ↗
    ›Feb 28, 2025approval530d agoIMFINZI (DURVALUMAB) — FDA approvalASTRAZENECA PLC

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

    full page →fda approvals ↗
    ›Feb 28, 2025approval530d agoOSENVELT (DENOSUMAB-BMWO) — FDA approvalOSENVELT

    Sponsor: CELLTRION INC. Form: INJECTABLE. Route: INJECTION

    full page →OSENVELT →fda approvals ↗
    ›Feb 28, 2025approval530d agoEPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (EPINEPHRINE BITARTRATE) — FDA approvalepinephrine bitartrate

    Sponsor: BAXTER HLTHCARE CORP. Form: SOLUTION. Route: INTRAVENOUS

    full page →epinephrine bitartrate →fda approvals ↗
    ›Feb 28, 2025approval530d agoULTOMIRIS (RAVULIZUMAB-CWVZ) — FDA approvalAlexion Pharmaceuticals Inc

    Sponsor: ALEXION PHARM. Form: INJECTABLE. Route: INJECTION

    full page →fda approvals ↗
    ›Feb 28, 2025device 510k530d agoRb Health (Us), LLC — Durex Polyisoprene Condom (510k cleared)Bausch Health US LLC

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

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoGt Metabolic Solutions, Inc. — MagDI System (MAG-02, DS-01) (510k cleared)Seed Health Inc

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

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoBasis Medical — Seclusion Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoQingdao Kingon Medical Science and Technology Co., Ltd. — Portable Oxygen Concentrator (P2-TOC) (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoPhenox Limited — pRESET Delta Thrombectomy Device and pRESET Delta LITE Thrombectomy Device (510k cleared)

    Product code: POL. Advisory committee: Neurology. Type: Special

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoShandon Diagnostics Limited — E1000 Dx Digital Pathology Solution (510k cleared)

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

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoBaxter Healthcare Corporation — Intravascular Extension Sets and Accessories (510k cleared)Baxter Healthcare Corp

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

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoFresenius Medical Care Renal Therapies Group, LLC — FX CorAL 60 (F00012969); FX CorAL 80 (F00012970); FX CorAL 100 (F00012971); FX CorAL 120 (F00012972); FX CorAL 600 (F00012973); FX CorAL 800 (F00012974); FX CorAL 1000 (F00012975) (510k cleared)Fresenius Medical Care AG

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

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoQIAGEN GmbH — QIAstat-Dx GI Panel 2 Mini B (510k cleared)

    Product code: PCH. Advisory committee: Microbiology. Type: Special

    full page →fda device 510k ↗
    ›Feb 28, 2025device 510k530d agoHeroic Faith International , Ltd. — Airmod (510k cleared)TH International Ltd

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

    full page →fda device 510k ↗
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    $LBRX45.52-0.72%
    $LBRX45.52-0.72%
    $LBRX45.52-0.72%
    $KMTS20.35+8.13%
    $XOSWW
    $ALKS49.18-0.45%
    $TMO447.81+1.31%
    $ELUT
    $AZN159.50-1.49%
    $FMS23.94-1.68%
    $THCH