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21,416 catalysts · 4,728 grant · 3,882 device 510k · 3,153 8k filing · 3,057 approval · 2,000 device pma · 2,000 device recall

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2026-08-10: 0 catalysts2026-08-11: 0 catalysts2026-08-12: 46 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: 3 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: 9 catalysts2026-11-03: 18 catalysts2026-11-04: 22 catalysts2026-11-05: 37 catalysts2026-11-06: 2 catalysts2026-11-07: 0 catalysts2026-11-08: 0 catalysts
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  • grant4,728
  • device 510k3,882
  • 8k filing3,153
  • approval3,057
  • device pma2,000
  • device recall2,000
device adverse event
1,000
  • recall931
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Mar 10, 2025

    18
    ›Mar 14, 2025device 510k517d agoCenters for Disease Control and Prevention — CDC Human Influenza Virus Real-time RT-PCR Diagnostic Panel: Influenza A/B Typing Kit (VER 2); Influenza A Subtyping Kit (VER 4); Influenza B Lineage Genotyping Kit (VER 1.1 and 2); and Influenza A/H5 Subtyping Kit (VER 4) (510k cleared)Hubei Provincial Center for Disease Control and Prevention

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoNexxt Spine — NEXXT MATRIXX® SI System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoArrow International, LLC (A subsidiary of Teleflex, Inc.) — Arrow™ Endurance™ Extended Dwell Peripheral Catheter System (EDC-00818) (510k cleared)Arrow International LLC

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoAidite (Qinhuangdao) Technology Co., Ltd. — Porcelain Powder (Enamel/ Modifier,Stain/Glaze,Stain/Glaze-A,Modeling Fluid ) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoKettenbach GmbH & Co. KG — Visalys® Bulk Fill 1 x 4 g Syringe (15060); Visalys® Bulk Fill 15 x 0.25 g Caps (15062); Visalys® Bulk Flow 1 x 2 g Syringe (15064); Visalys® Bulk Flow 15 x 0.25 g Caps (15066); Visalys® Bulk Flow Intro pack (15067); Visalys® Bulk Intro pack (15068) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoKorot Co., Ltd. — KOROT Blood Pressure Monitor (KOROT P3 Accurate) (510k cleared)Kowa Co Ltd

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoLumea, Inc. — Viewer+ (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoBaxter Healthcare Corporation — Solution Administration Sets (510k cleared)Baxter Healthcare Corp

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoArthrex, Inc. — Arthrex 4.75 mm Double Loaded Knotless Corkscrew Suture Anchor (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoNeurologica Corporation, A Subsidiary of Samsung — BodyTom 64 (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoMediclus Co., Ltd. — One-Fil Putty (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoNox Medical Ehf — DeepRESP (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoPromisemed Hangzhou Meditech Co., Ltd. — Promisemed Safety Huber Needles (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agobioMerieux, Inc. — VITEK COMPACT PRO (510k cleared)BIOMERICA INC

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoMonogram Orthopaedics, Inc. — mBôs (Monogram mBôs TKA System) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoMoon Surgical — Maestro System (REF100) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 14, 2025device 510k517d agoPenumbra, Inc. — Ruby XL System (510k cleared)Penumbra Inc

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

    full page →fda device 510k ↗
    ›Mar 16, 2025device 510k515d agoContract Medical International, GmbH — Catapult Guide Sheath; 4F; 15cm (US-34015-F-ST-H); Catapult Guide Sheath; 4F; 45cm (US-34045-F-ST-H); Catapult Guide Sheath; 4F; 60cm (US-34060-F-ST-H); Catapult Guide Sheath; 4F; 90cm (US-34090-F-ST-H); Catapult Guide Sheath; 4F; 130cm (US-34130-F-ST-H); Catapult Guide Sheath; 5F; 15cm (US-35015-F-ST-H); Catapult Guide Sheath; 5F; 45cm (US-35045-F-ST-H); Catapult Guide Sheath; 5F; 45cm; Hockey Stick (US-35045-F-HS-H); Catapult Guide Sheath; 5F; 45cm; Multipurpose (US-35045-F-MP-H); Ca (510k cleared)

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

    full page →fda device 510k ↗

    Week of Mar 17, 2025

    32
    ›Mar 17, 2025approval514d agoAMNESTEEM (ISOTRETINOIN) — FDA approvalMylan Pharmaceuticals Inc

    Sponsor: MYLAN PHARMS INC. Form: CAPSULE. Route: ORAL

    full page →fda approvals ↗
    ›Mar 17, 2025approval
    ← prev
    page 12 of 429
    next →
    514d ago
    IMULDOSA (USTEKINUMAB-SRLF) — FDA approvalustekinumab biosimilar

    Sponsor: ACCORD BIOPHARMA INC.. Form: INJECTABLE. Route: INTRAVENOUS

    full page →ustekinumab biosimilar →fda approvals ↗
    ›Mar 17, 2025device 510k514d agoCarlsmed, Inc. — aprevo® anterior and lateral lumbar interbody fusion device, aprevo® anterior lumbar interbody fusion device with interfixation (510k cleared)CARLSMED, INC.

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoCranial Technologies, Inc. — DOC Band 3D (510k cleared)Q/C TECHNOLOGIES, INC.

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoLagis Enterprise Co., Ltd. — LAGIS Suction Irrigation System (510k cleared)Cre8 Enterprise Ltd

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoServ Medical Pte., Ltd. — SERV MEDICAL CDSS (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoDia Imaging Analysis, Ltd. — LVivo Software Application (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoJiale Health Technology Shenzhen Co., Ltd. — Air Compression Leg Massager (K-705) (510k cleared)Aimei Health Technology Co., Ltd.

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoThe Magstim Company Limited — Horizon® 3.0 TMS Therapy System (Horizon 3.0 Inspire); Horizon® 3.0 TMS Therapy System (Horizon 3.0 with StimGuide Pro); Horizon® 3.0 TMS Therapy System (Horizon 3.0) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoOrthonovis, Inc. — BPS Wrist Fracture System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoGe Medical Systems, LLC — SIGNA Prime Elite (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoZiehm Imaging GmbH — Ziehm Solo FD (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoSpecialty Water Technologies, Inc. — UPT Series Medical RO Water Treatment System (510k cleared)WATTS WATER TECHNOLOGIES INC

    Product code: FIP. Advisory committee: Gastroenterology, Urology. Type: Special

    full page →fda device 510k ↗
    ›Mar 17, 2025device 510k514d agoCentervue S.P.A. — MAIA (AHMACME001) (510k cleared)

    Product code: MYC. Advisory committee: Ophthalmic. Type: Traditional

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoKlarity Medical & Equipment (GZ) Co., Ltd. — Klarity SGRT System (ARSG-E1A, ARSG-E3A) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoWhip Mix Corporation — Hard Splint & Thermo-Adaptive Splint (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoOsteoCentric Technologies — The OsteoCentric Bone Plate and Screw System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoIray Imaging Technology (Haining) Limited — Lux HD 35 Detector (Lux HD 35); Lux HD 43 Detector (Lux HD 43) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoShenzhen Perfect Idea Technology Limited — Aglaia LED Beauty Device (BP-D2309) (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoTeleflex Medical — QuikClot Control+ Hemostatic Device (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoVy Spine, LLC — FortiVy™ OsteoVy™ Lumbar IBF (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoBetter Care Plastic Technology Co., Ltd. — Powder Free Nitrile Patient Examination Gloves, Blue Colored, Non Sterile, Low Dermatitis Potential. Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (510k cleared)Teva Pharmaceuticals USA Inc

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoGlobal Healthcare SG Sdn. Bhd — CarbonCool® System (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoOlympus Medical Systems Corp. — Single Use Retrieval Basket V FG-V421PR/V422PR/V431P/V432P (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoRadlink, Inc. — Radlink GPS Pro Imaging (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoHangzhou Laihe Biotech Co., Ltd. — LYHER® Oral fluid Multi-Drug Test Kit (Cube) (510k cleared)Hangzhou DAC Biotech Co Ltd

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

    full page →fda device 510k ↗
    ›Mar 18, 2025device 510k513d agoQuibim S.L. — QP-Prostate® CAD (510k cleared)

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

    full page →fda device 510k ↗
    ›Mar 19, 2025approval512d agoKEYTRUDA (PEMBROLIZUMAB) — FDA approvalpembrolizumab

    Sponsor: MERCK SHARP DOHME. Form: SOLUTION. Route: INTRAVENOUS

    full page →pembrolizumab →fda approvals ↗
    ›Mar 19, 2025approval512d agoMEKINIST (TRAMETINIB) — FDA approvalSpexotras

    Sponsor: NOVARTIS. Form: SOLUTION. Route: ORAL

    full page →Spexotras →fda approvals ↗
    ›Mar 19, 2025approval512d agoTAFINLAR (DABRAFENIB MESYLATE) — FDA approvaldabrafenib mesylate ODT

    Sponsor: NOVARTIS. Form: CAPSULE. Route: ORAL

    full page →dabrafenib mesylate ODT →fda approvals ↗
    ›Mar 19, 2025approval512d agoMEKINIST (TRAMETINIB DIMETHYL SULFOXIDE) — FDA approvalSpexotras

    Sponsor: NOVARTIS. Form: TABLET. Route: ORAL

    full page →Spexotras →fda approvals ↗
    ›Mar 19, 2025approval512d agoTAFINLAR (DABRAFENIB MESYLATE) — FDA approvaldabrafenib mesylate ODT

    Sponsor: NOVARTIS. Form: CAPSULE. Route: ORAL

    full page →dabrafenib mesylate ODT →fda approvals ↗
    $PEN324.29-0.11%
    $BMRA
    $NVS152.51-1.35%
    $AFJKU
    $QCLS
    $ABVC
    $NVS152.51-1.35%
    $CRE
    $WTS
    $CARL
    $NVS152.51-1.35%
    $NVS152.51-1.35%