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19,642 catalysts · 4,728 grant · 3,189 8k filing · 2,737 device 510k · 2,721 approval · 2,000 device recall · 1,916 device pma

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  • grant4,728
  • 8k filing3,189
  • device 510k2,737
  • approval2,721
  • device recall2,000
  • device pma1,916
device adverse event
1,000
  • recall686
  • earnings584
  • phase 2 completion172
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    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jun 23, 2025

    50
    ›Jun 24, 2025approval415d agoRALDESY (TRAZODONE HYDROCHLORIDE) — FDA approvalTeva Pharmaceuticals USA Inc

    Sponsor: KAMAT. Form: SOLUTION. Route: ORAL

    full page →fda approvals ↗
    ›Jun 24, 2025device pma415d agoDePuy Orthopaedics, Inc. — CERAMAX® ceramic total hip system (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MRA. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Jun 24, 2025device pma415d agoDepuy, Inc. — LCS® Total Knee System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NJL. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Jun 24, 2025device pma415d agoABBOTT MEDICAL — Liberta RC™ Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MHY. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Jun 24, 2025device pma415d agoABBOTT MEDICAL — Eterna™ Spinal Cord Stimulation (SCS) Implantable Pulse Generator (IPG) (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LGW. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Jun 24, 2025device pma415d agoBiomet Manufacturing Corp — OXFORD(TM) MENISCAL UNICOMPARTMENTAL KNEE SYSTEM (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NRA. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Jun 24, 2025device pma415d agoStryker Neurovascular — Neuroform Atlas® Stent System (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 24, 2025device 510k415d agoProsidyan, Inc. — GPS Advanced; GPS Advanced Cannula (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 24, 2025device 510k415d agoPro Surgical, Inc. — ProAM ALIF System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 24, 2025device 510k415d agoPhilips Image Guided Therapy Devices — Bridge Plus Occlusion Balloon (590-002) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 24, 2025device 510k415d agoHypervision Surgical — HyperSnap Surgical System (HSS) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 24, 2025device 510k415d agoImagine Milling Technologies, LLC — MIST IC (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 24, 2025device 510k415d agoOrthoPediatrics Corp. — PediFlex™ Flexible Nail System (510k cleared)ORTHOPEDIATRICS CORP

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

    full page →fda device 510k ↗
    ›Jun 24, 2025device 510k415d agoSpectrum Medical S.R.L. — Quantum Perfusion Centrifugal Blood Pump CP22NG with Integrated Sensors (CP22V-NG) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025approval414d agoMETHADONE HYDROCHLORIDE — FDA approvalMETHADONE HYDROCHLORIDE

    Sponsor: HIKMA. Form: TABLET. Route: ORAL

    full page →METHADONE HYDROCHLORIDE →fda approvals ↗
    ›Jun 25, 2025recall414d agoUmary-USA.com recall (Cls I)OCULAR THERAPEUTIX, INC

    UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295 — Reason: Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone, Diclofenac and Omeprazole. — Status: Completed

    full page →fda recalls ↗
    ›Jun 25, 2025recall414d agoAurobindo Pharma USA Inc recall (Cls II)Aurobindo Pharma USA Inc

    Acetaminophen Tablets, 325 mg, 100-count bottles, Distributed by: Amazon.com Services LLC, 410 Terry Avenue N., Seattle, WA 98109, NDC 72288-405-10 — Reason: cGMP deviations: Due to confirmed consumer complaints received with the observation of tablet discoloration (brown surface on tablets). — Status: Ongoing

    full page →fda recalls ↗
    ›Jun 25, 2025recall414d agoEugia US LLC recall (Cls II)Eugia US LLC

    Gentamicin Injection, USP, (PEDIATRIC), 20 mg per 2 mL (10 mg per mL*), 2 mL Single-Dose Vial, Rx Only, Mfd. in India for: Eugia US LLC, E. Windsor, NJ, 08520 Vial- NDC 55150-401-01, Carton NDC 55150-401-25 — Reason: Failed Stability Specifications: Out of specification results for the Color Absorbance test during 12 Month sample analysis. — Status: Ongoing

    full page →fda recalls ↗
    ›Jun 25, 2025recall414d agoUmary-USA.com recall (Cls I)OCULAR THERAPEUTIX, INC

    UMOVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7503046054134 — Reason: Marketed without approved NDA/ANDA- Laboratory analysis found product to be tainted with undeclared ingredients: Dexamethasone and Diclofenac. — Status: Completed

    full page →fda recalls ↗
    ›Jun 25, 2025device pma414d agoBoston Scientific Corp — Precision Spinal Cord Stimulator (SCS) Systems (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: LGW. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoBoston Scientific Corp — VERCISE DEEP BRAIN STIMULATION (DBS)SYSTEM (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 30-Day Notice. Product code: NHL. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoBiotronik Nro, Inc. — Prospera Spinal Cord Stimulation (SCS) System, Resilience Percutaneous Lead, HomeStream Remote Management (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: LGW. Advisory committee: NE. Decision: APPR

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoEndotronix, Inc. — Cordella Pulmonary Artery Sensor System (CorPASS) (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoNeuros Medical, Inc. — Altius Direct Electrical Nerve Stimulation System (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: SAZ. Advisory committee: NE. Decision: APPR

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoAllergan — Juvederm Injectable Gel (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: LMH. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoABBOTT MEDICAL — MitraClip™ G4 Clip Delivery System; MitraClip™ NTR Clip Delivery System; MitraClip™ XTR Clip Delivery System (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoSyncardia Systems, LLC — Total Artificial Heart (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 25, 2025device pma414d agoABBOTT MEDICAL — TriClip™ G4 Delivery System; MitraClip™ G5 Delivery System, TriClip™ G5 Delivery System (PMA supplement)

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

    full page →fda device pma ↗
    ›Jun 25, 2025device 510k414d agoCg Medtech Co., Ltd. — ANAX™ OCT Spinal System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoPrismatik Dentalcraft, Inc. — Flexible Partial Resin (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoS&G Biotech, Inc. — EGIS Biliary Double Bare Stent (BDB080405) (510k cleared)IO Biotech, Inc.

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoSysmex America, Inc. — Sysmex XR-Series (XR-20) Automated Hematology Analyzer (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoShenzhen Kaiyan Medical Equipment Co., Ltd. — CurrentBody Skin™ LED Light Therapy Mask Series 2 (MK-90H) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoSmith & Nephew, Inc. — BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (cobraid blue); BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (cobraid black); BIORAPTOR 2.3 PK Suture Anchor w/ ULTRABRAID (#2) Suture (white); BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (cobraid black); BIORAPTOR CURVED 2.3 PK Suture Anchor w/ ONE 38 ULTRABRAID (#2) Suture (cobraid blue) (510k cleared)SMITH & NEPHEW PLC

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoExpanding Innovations, Inc. — X-PAC® LLIF Expandable Lateral Cage System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoEnraf-Nonius, B.V. — Curapuls 670 (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoStrait Access Technologies Holdings — SAT CenterFlow Molding Balloon Catheter (IN20-00313) (510k cleared)SS&C Technologies Holdings Inc

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoBlue Belt Technologies, Inc. — CORIOGRAPH Pre-Op Planning and Modeling Services (510k cleared)BETA Technologies, Inc.

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoPAJUNK GmbH Medizintechnologie — SPROTTE® STANDARD (LUER/ NRFit®) Lumbar Puncture (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoSysmex America, Inc. — Sysmex XR-Series (XR-10) Automated Hematology Analyzer (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoGeniphys, Inc. — GeniPhys Collymer Self-Assembling Scaffold (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoFisher & Paykel Healthcare, Ltd. — Optiflow+ Nasal Cannula - Small (OPT942); Optiflow+ Nasal Cannula - Medium (OPT944); Optiflow+ Nasal Cannula - Large (OPT946); Optiflow+ Nasal Cannula Small (MYOPT9SMALL); Optiflow+ Nasal Cannula Medium (MYOPT9MEDIUM); Optiflow+ Nasal Cannula Large (MYOPT9LARGE) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoKardium, Inc. — Globe® Pulsed Field System (510k cleared)Kardigan Inc

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

    full page →fda device 510k ↗
    ›Jun 25, 2025device 510k414d agoAnhui Jbh Medical Apparatus Co., Ltd. — Power Wheelchair (D26) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jun 26, 2025approval413d agoPUR-WASH (PURIFIED WATER) — FDA approval

    Sponsor: NIAGARA PHARMS. Form: SOLUTION. Route: OPHTHALMIC

    full page →fda approvals ↗
    ›Jun 26, 2025approval413d agoCAPRELSA (VANDETANIB) — FDA approvalvandetanib

    Sponsor: GENZYME CORP. Form: TABLET. Route: ORAL

    full page →vandetanib →fda approvals ↗
    ›Jun 26, 2025device pma413d agoMerz North America, Inc. — RADIESSE® Injectable Implant (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LMH. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Jun 26, 2025device pma413d agoMedtronic — HeartWare­™ Ventricular Assist System (HVAD) (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Jun 26, 2025device pma413d agoMedtronic, Inc. — Freestyle Bioprosthesis, Models 995, 995CS, 995MS (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Jun 26, 2025device pma413d agoBoston Scientific Corporation — Ranger™ Paclitaxel-Coated PTA Balloon Catheter (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: 135 Review Track For 30-Day Notice. Product code: ONU. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
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