BEUDAMED
    46 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    AtriClip FLEX-V

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·Gore Carotid Stent

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008361·PedFuse Respond, CNL, 5.0mm x 40mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008330·Pedicle Screw Assy. 5mm Respond

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008385·PedFuse Respond, CNL, 5.0mm x 50mm

    Batrik Arc Wire Brushes Single Use

    FDA UDI
    Batrik Medical Manufacturing Inc·00690521008960·Brush/Red/BD 10mm/BL 50mm/OL 75cm - Rigid - SIN...

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008323·Pedicle Screw Assy. 5mm Respond

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008354·PedFuse Respond, CNL, 5.0mm x 35mm

    Sorrento Bioglass 10cc (100 x 20 x 5 mm)

    FDA UDI
    XENCO MEDICAL LLC·B064HB1180010·

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008347·PedFuse Respond, CNL, 5.0mm x 30mm

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008378·PedFuse Respond, CNL, 5.0mm x 45mm

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K1100100·Tray Insert

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K1100100·Tray Insert

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100100·Tray Insert 3, Cosmolock, Arcamed

    HDL CHOLESTEROL (HDLX) ASSAY

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NOCC HYDROPHILIC WOUND DRESSING

    FDA 510(k)
    FDA Unclassified ·Unknown

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·GORE Carotid Stent

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·GORE Carotid Stent

    Stent, Carotid

    FDA Pre-Market Approval
    FDA Class 3 ·GORE Carotid Stent

    LIGACLIP MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·LACEY MANUFACTURING CO·Product code GDO·July 28, 2000