BEUDAMED
    666 results · 20ms · Sources: EU EUDAMED, US FDA

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    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·NUVASIVE PCM CERVICAL DISC SYSTEM

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·NUVASIVE PCM CERVICAL DISC SYSTEM

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·NUVASIVE PCM CERVICAL DISC

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·NU VASIVE PCM CERVICAL DISC SYSTEM

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·NUVASIVE'S PCM CERVICAL DISC

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·PCM CERVICAL DISC

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·NUVASIVE'S PCM CERVICAL DISC

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·NuVasive PCM Cervical Disc

    RHEAD

    FDA UDI
    Stryker GmbH·00886385022796·Lateral Assembly, Radial Head Implant, Size 3

    Mini Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746105586·DB BKT MINI MS HGW LL 1ST BIC 018 T-12 A+2 R=0

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694001168·18mm Left L Plate

    DURAVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948004618·DURAVENT, SIZE 12

    SAVANNAH

    FDA UDI
    SPINAL ELEMENTS·00840916151256·SAVANNAH®-T TAB BREAKER

    MAXFRAME

    FDA UDI
    SYNTHES (U.S.A.) LP·10886982338594·MAXFRAME AUTOSTRUT(TM) HEXAPOD STRUT - SHORT

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193107851·HA PEEK EVOS Straight, ,12mmx8mmx 22mm , FLAT ...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694033107·Mini 18mm Left L Plate, Sterile

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694063029·2.0 System 4 Hole 18mm Left L Plate Sterile Qty 5

    GRYPHON T BR DS ANCHOR W/ORTHOCORD, GRYPHON T BR ANCHOR W /ORTHOCORD, GRYPHON P BR DS ANCHOR W/ORTHOCORD, GRYPHON P BR A

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·April 7, 2026

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·April 7, 2026