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18,496 catalysts · 4,728 grant · 3,230 8k filing · 2,654 approval · 2,246 device 510k · 1,812 device recall · 1,561 device pma

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  • grant4,728
  • 8k filing3,230
  • approval2,654
  • device 510k2,246
  • device recall1,812
  • device pma1,561
device adverse event
1,000
  • recall600
  • earnings584
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    • Oncology148
    • Infectious Disease46
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    • Pulmonology22
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    Week of Jul 28, 2025

    50
    ›Jul 30, 2025device pma380d agoCentinel Spine, LLC — prodisc L (PMA supplement)

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

    full page →fda device pma ↗
    ›Jul 30, 2025device pma380d agoBausch & Lomb, Inc. — enVista Envy™ hydrophobic acrylic intraocular lens (IOL), enVista Envy™ toric hydrophobic acrylic intraocular lens (IOL) (PMA supplement)Bausch & Lomb Corp

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

    full page →fda device pma ↗
    ›Jul 30, 2025device pma380d agoVascutek, Ltd. — Thoraflex™ Hybrid (PMA supplement)

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

    full page →fda device pma ↗
    ›Jul 30, 2025device pma380d agoCentinel Spine, LLC — prodisc® C (PMA supplement)

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

    full page →fda device pma ↗
    ›Jul 30, 2025device recall380d agoMckesson Medical-Surgical Inc. Corporate Office device recall (Cls II)

    Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020 — Reason: Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 30, 2025device recall380d agoS.I.N. Implant System Ltda device recall (Cls II)

    IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N; IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N; IMPLANT EPIKUT PLUS MT16 3,5X13,0MM, REF: ILM 3513N; IMPLANT EPIKUT PLUS MT16 3,5X15,0MM, REF: ILM 3515N; IMPLANT EPIKUT PLUS MT16 3,8X10,0MM, REF: ILM 3810N; IMPLANT CM16 3,8 X 11MM, REF: ILM 3811N; IMPLANT EPIKUT PLUS MT16 3,8X15,0MM, REF: ILM 3815N; IMPLANT EPIKUT PLUS MT16 4,0X10,0MM, REF: ILM 4010N; IMPLANT EPIKUT PLUS MT16 4,0X11,5MM, REF: ILM 4011N; IMPLANT EPIKUT PLUS MT16 4,0X13,0MM, REF: ILM 4013N; IMP EPIKUT PLUS LONG MT16 4,0X20,0MM, RES: ILM 4020N; IMPLANT EPIKUT PLUS MT16 4,0X8,5MM, RES: ILM 4085N; IMPLANT EPIKUT PLUS MT16 4,5X13,0MM, REF: ILM 4513N; IMPLANT EPIKUT PLUS MT16 4,5X15,0MM, REF: ILM 4515N; IMPLANT EPIKUT PLUS MT16 4,5X8,5MM, REF: ILM 4585N; IMPLANT EPIKUT PLUS MT16 5,0X10,0MM, REF: ILM 5010N; IMPLANT EPIKUT PLUS MT16 5,0X11,5MM, REF: ILM 5011N; IMPLANT EPIKUT PLUS MT16 4,5X10,0MM, REF: ILM 4510N; IMPLANT EPIKUT PLUS MT16 5,0X13,0MM, RES: ILM 5013N; IMPLANT EPIKUT PLUS MT16 5,0X15,0MM, REF: ILM 5015N; IMPLANT EPIKUT PLUS MT16 5,0X8,5MM, REF: ILM 5085N; IMP EPIKUT PLUS LONG MT16 4,0X18,0MM, REF: ILM 4018N; IMP EPIKUT PLUS LONG MT16 3,8X18,0MM, REF: ILM 3818N; IMPLANT EPIKUT PLUS MT16 4,5X11,5MM, REF: ILM 4511N; IMPLANT EPIKUT MT16 4,5X15,0MM, REF: ILM 4515; IMPLANT EPIKUT MT16 4,5X8,5MM, REF: ILM 4585; IMPLANT EPIKUT MT16 3,8X13,0MM, REF: ILM 3813; IMPLANT EPIKUT MT16 3,8X15,0MM, REF: ILM 3815; IMPLANT EPIKUT MT16 5,0X8,5MM, REF: ILM 5085; IMPLANT EPIKUT MT16 3,8X11,5MM, REF: ILM 3811; IMPLANT EPIKUT PLUS MT16 3,8X20,0MM, REF: ILM 3820N; IMPLANT EPIKUT PLUS MT16 4,5X18,0MM, REF: ILM 4518N; IMPLANT UNITITE MORSE COMPACT 6.0X7MM, REF: UCMC 6007N — Reason: Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which could compromise product quality and performance. — Status: Ongoing

    ›Jul 30, 2025device recall380d agoContract Medical International GmbH device recall (Cls II)

    Brand Name: Fortress Introducer Sheath System Product Name: Fortress Introducer Sheath System Model/Catalog Number: 386594 Product Description: Fortress Introducer Sheath System, 6F Straight 45cm: — Reason: Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 30, 2025device 510k380d agoShenzhen Lifotronic Technology Co., Ltd. — Diode Laser Hair Removal Machine (models: T60A, T60B, T60C, T60D, T60E) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k380d agoABBOTT MEDICAL — EnSite™ X EP System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k380d 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 510k380d 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 510k380d 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 510k380d agoSpectrum Vascular — Intraosseous Infusion Needles (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k380d agoTsk Laboratory, Japan — TSK Syringe (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k380d 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 510k380d 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 510k380d 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 510k380d agoHydrocision, Inc. — SpineSite Endoscope System (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k380d 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 510k380d agoTonica Elektronik A/S — T65 (9016E061-) (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 30, 2025device 510k380d 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 510k380d 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 510k380d 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, 2025approval379d agoSPRAVATO (ESKETAMINE HYDROCHLORIDE) — FDA approvalJanssen Therapeutics

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

    full page →fda approvals ↗
    ›Jul 31, 2025approval379d agoLEQVIO (INCLISIRAN SODIUM) — FDA approvalinclisiran

    Sponsor: NOVARTIS. Form: SOLUTION. Route: SUBCUTANEOUS

    full page →inclisiran →fda approvals ↗
    ›Jul 31, 2025device pma379d 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 pma379d 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 recall379d 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 recall379d 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 recall379d 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 recall379d 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 recall379d 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 recall379d 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 recall379d 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 510k379d 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 510k379d 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 510k379d 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 510k379d 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 510k379d 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 510k379d 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 510k379d 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 510k379d agoLutronic Corporation — eCO2 3D (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k379d 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 510k379d agoAmbulatory Monitoring, Inc. — Sleep Watch (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k379d agoArtera, Inc. — ArteraAI Prostate (510k cleared)Arteris, Inc.

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k379d agoSiemens Medical Solutions — YSIO X.pree (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k379d agoRemedi, Inc. — REMEX Xcam6 (510k cleared)

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

    full page →fda device 510k ↗
    ›Jul 31, 2025device 510k379d 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, 2025approval378d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
    ›Aug 1, 2025approval378d agoMETHYLPREDNISOLONE — FDA approvalMEDROL

    Sponsor: SANDOZ. Form: TABLET. Route: ORAL

    full page →MEDROL →fda approvals ↗
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    full page →fda device recalls ↗
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    $BLCO16.89+0.78%
    $FRTRY
    $AIP
    $NVS152.24-0.06%
    $COO
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