BEUDAMED
    61 results · 27ms · 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 ×

    TIGR Matrix Surgical Mesh

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

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376632827·TL VBR EXP TRIAL EP, BAN 16x30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376633329·TL VBR SIZING TIP, BAN 16x30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376513836·TL VBR DISTRACTOR TIP, BAN 16x30mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376518992·12 mm CORE ENDPLATE, LAT 16 x 30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376519951·16 mm CORE ENDPLATE, LAT 16 x 30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376521589·12 mm CORE ENDPLATE, BAN 16 x 30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376521220·16 mm CORE ENDPLATE, BAN 16 x 30 mm 5°

    BIO PLUG

    FDA UDI
    Biomet Orthopedics, LLC·00880304004078·

    STRYKER T6 HOODS AND TOGAS

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

    DDRVERSA MOTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376658490·16mm CORE, NANOTEC BAN 16 x 30mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376657530·16mm CORE, NANOTEC LAT 16 x 30mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376668185·12mm CORE, NANOTEC KBN 16 x 30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376667799·12mm CORE, NANOTEC BAN 16 x 30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376669755·12mm CORE, NANOTEC LAT 16 x 30 mm 5°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376663326·16mm CORE, NANOTEC KBN 16 x 30mm 5°

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 25, 2025

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·July 15, 2011

    RESTORE

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 11, 2013