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19,858 catalysts · 4,728 grant · 3,301 8k filing · 2,785 device 510k · 2,724 approval · 2,000 device recall · 1,962 device pma

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  • grant4,728
  • 8k filing3,301
  • device 510k2,785
  • approval2,724
  • device recall2,000
  • device pma1,962
device adverse event
1,000
  • recall693
  • earnings584
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Jul 28, 2025

    50
    ›Jul 30, 2025device 510k381d agoProvidence Medical Technology, Inc. — CORUS™ Navigation System-GX (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoRiverpoint Medical — Iconix Speed Anchor; Iconix Speed HA+ Anchor (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoE.O.S Co., Ltd. — P-CON (polymacon) Soft (hydrophilic) Contact Lenses (Tinted, Color) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoSpectrum Vascular — Intraosseous Infusion Needles (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoTsk Laboratory, Japan — TSK Syringe (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoChangsha Anxiang Medical Technology Co., Ltd. — TENS and EMS Unit (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoHartalega NGC Sdn. Bhd. — Sterile Nitrile Powder Free Examination Glove Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (Blue); Sterile Nitrile Powder Free Examination Glove Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (Blue) – Extended Cuff (510k cleared)Teva Pharmaceuticals USA Inc

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoHermes Medical Solutions AB — Voxel Dosimetry (00859873006226) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoHydrocision, Inc. — SpineSite Endoscope System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoCardio Ring Technologies, Inc. Taiwan Branch — ArteVu (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoTonica Elektronik A/S — T65 (9016E061-) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoTyber Medical, LLC — Tyber Medical Distal Radius Plating System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoSuzhou Zenith Vascular SciTech Limited — Micro Catheter (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k381d agoAcuity Surgical Devices, LLC — Stabilis SA Cervical Stand-Alone System (Various PNs) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025approval380d agoSPRAVATO (ESKETAMINE HYDROCHLORIDE) — FDA approvalJanssen Therapeutics

    Sponsor: JANSSEN PHARMS. Form: SPRAY. Route: NASAL

    full page →fda approvals ↗
    ›Jul 31, 2025approval380d agoLEQVIO (INCLISIRAN SODIUM) — FDA approvalinclisiran

    Sponsor: NOVARTIS. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →inclisiran →fda approvals ↗
    ›Jul 31, 2025device pma380d agoThe Cooper Companies — Biomedics 55 Asphere; Biomedics Toric (PMA supplement)COOPER COMPANIES, INC.

    Supplement type: 30-Day Notice. Product code: LPM. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Jul 31, 2025device pma380d agoVentana Medical Systems, Inc. — CINtec PLUS Cytology (PMA supplement)MERIT MEDICAL SYSTEMS INC

    Supplement type: Real-Time Process. Product code: QKF. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Jul 31, 2025device recall380d agoLumicell, Inc. device recall (Cls II)

    Brand Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Product Name: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Model/Catalog Number: 900-00218 Sterile Cover 10-Pack Shipper Box Assembly Software Version: Not Applicable Product Description: Sterile Cover Component: Lumicell Direct Visualization System (DVS) / PMA # P230014 — Reason: The potential of the elastic bands included in the kit detaching or fracturing during surgical procedures. As a result, these failures may pose a risk of retained foreign bodies in the surgical cavity and potentially leading to surgical site infections. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 31, 2025device recall380d agoMedline Industries, LP device recall (Cls I)

    Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH 401600RH 401603RH 401606RH 401652RH 401653RH 401654RH 401904RH 401905RH 401908RH 401914RH 401915RH 401918RH 401932RH 401933RH 401934RH 401938RH 401939RH 401940RH 401941RH 401991RH — Reason: Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 31, 2025device recall380d agoMedline Industries, LP device recall (Cls I)

    Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH — Reason: Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 31, 2025device recall380d agoMedline Industries, LP device recall (Cls I)

    Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH 81402RH 81404RH 81405RH 81472RH 81473RH 81474RH 81531RH 81532RH — Reason: Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 31, 2025device recall380d agoMedline Industries, LP device recall (Cls I)

    Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart. For imaging guidance only, not treatment delivery, during cardiac interventional percutaneous procedures. Medline Item Numbers 10135910RH 10135936RH — Reason: Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 31, 2025device recall380d agoWaldemar Link GmbH & Co. KG (Mfg Site) device recall (Cls II)

    LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. 5, CoCrMo/TiNbN, cemented, Fixed. REF Number: 880-100/50 — Reason: Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 31, 2025device recall380d agoMedline Industries, LP device recall (Cls I)

    Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH — Reason: Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 31, 2025device 510k380d agoUnited Orthopedic Corporation — U2 Total Knee System – PF+ Patella; USTAR II System– PF+ Patella (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoMedacta International S.A. — Mpact Constrained Liner (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoZimmer Biomet — Trabecular Metal Acetabular Revision System, Acetabular Liners and Constrained Liners (510k cleared)ZIMMER BIOMET HOLDINGS, INC.

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoSiemens Medical Solutions USA, Inc. — Biograph Trinion (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoShenzhen TPH Technology Co., Ltd. — Wearable Breast Pump (Model FS12A); Wearable Breast Pump (Model FS12B) (510k cleared)Fortior Technology (Shenzhen) Co., Ltd./ADR

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoHologic, Inc. — Genius AI Detection 2.0 (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoRoche Molecular Systems, Inc. — cobas Respiratory 4-flex for use on the cobas 5800/6800/8800 Systems (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoLutronic Corporation — eCO2 3D (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoMedacta International S.A. — NextAR(TM) Spine (510k cleared)Stemedica International S.A.

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoAmbulatory Monitoring, Inc. — Sleep Watch (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoArtera, Inc. — ArteraAI Prostate (510k cleared)Arteris, Inc.

    Product code: SFH. Advisory committee: Pathology. Type: Direct

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoSiemens Medical Solutions — YSIO X.pree (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoRemedi, Inc. — REMEX Xcam6 (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k380d agoShenzhen Mindray Bio-Medical Electronics Co., Ltd. — BeneVision Central Monitoring System (510k cleared)

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

    full page →fda device 510k ↗
    ›Aug 1, 2025approval379d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
    ›Aug 1, 2025approval379d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
    ›Aug 1, 2025approval379d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
    ›Aug 1, 2025approval379d agoNURTEC ODT (RIMEGEPANT SULFATE) — FDA approvalrimegepant sulfate ODT

    Sponsor: PFIZER. Form: TABLET, ORALLY DISINTEGRATING. Route: ORAL

    full page →rimegepant sulfate ODT →fda approvals ↗
    ›Aug 1, 2025device pma379d agoAbiomed, Inc. — Impella 5.5 with SmartAssist System; Impella CP with SmartAssist System; Impella 2.5; Impella 5.0; Impella LD; (PMA supplement)Abion Inc

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

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoAbiomed, Inc. — Impella RP System; Impella RP with SmartAssist System; Impella RP Flex with SmartAssist System; (PMA supplement)Abion Inc

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

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoMedtronic, Inc. — AFR-00004 HexaGen RF Generator (RFG) and AFR-00008 HexaPulse PF Generator (PFG) (PMA supplement)Medtronic plc

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

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoDePuy Orthopaedics, Inc. — CERAMAX CERAMIC HIP SYSTEM (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoMedtronic Neuromodulation — InterStim™ Therapy System, Verify™ Evaluation System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: EZW. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoABBOTT MEDICAL — TactiFlex™ Ablation Catheter, Sensor Enabled™ (PMA supplement)

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

    full page →fda device pma ↗
    ›Aug 1, 2025device pma379d agoBoston Scientific Corp — AngioJet Thrombectomy System (PMA supplement)BOSTON SCIENTIFIC CORP

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

    full page →fda device pma ↗
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    $ZBH87.97+0.93%
    $PFE26.80+1.86%
    $NVS151.72-0.39%
    $FRTRY
    $AIP
    $MMSI90.50-0.77%
    $COO
    $MDT90.58-0.20%
    $BSX51.69+0.53%