BEUDAMED
    329 results · 21ms · Sources: EU EUDAMED, US FDA

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    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·HYLAFORM (HYLAN B GEL)

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·PREVELLE SILK

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·HYLAFORM, HYLAFORM PLUS, ND CAPTIQUE

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·HYLAFORM AND HYLAFORM PLUS

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·PREVELLE SILK

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·PREVELLE SILK

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·HYLAFORM PLUS (HYLAN B GEL)

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·HYLAFORM (HYLAN B GEL), HYLAFORM PLUS, CAPTIQUE

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·PREVELLE SILK & HYLAN B GEL

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·HYLAFORM (HYLAN B GEL); PREVELLE SILK

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·PREVELLE SILK

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·CAPTIQUE INJECTABLE GEL

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·HYLAFORM FAMILY DERMAL FILLERS (HYLAFORM, HYLAFORM PLUS AND CAPTIQUE INJECTABLE GEL)

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·PREVELLE SILK

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·PREVELLE SILK

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00885074163826·CASE 7030032 SCREW GAUGE

    STAR

    FDA UDI
    Stryker GmbH·00886385017068·RASP ASSEMBLY

    Humelock Reversed Shoulder

    FDA UDI
    FX SOLUTIONS·03701037307229·HUMELOCK REVERSED EXTRACTOR

    SCFE Screw

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132114155·4.0mm X 32mm MED THREAD CANNULATED SCREW

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2710420300320·Anterio Lateral Closing Wedge Osteotomy Guide, ...