BEUDAMED
    56 results · 21ms · 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 ×

    Calcium Salt Bone Void Filler, Drillable, Non-Screw Augmentation

    FDA Pre-Market Approval
    FDA Class 2 ·PRO OSTEON IMPLANT 500 HYDROXYAPATITE BONE VOID FILLER

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON IMPLANT 500 POROUS CORALLINE HYDROXYAPATITE BONE GRAFT SUBSTITUTE

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUE BLOCKS & GRANULES

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON 500 BONE GRAFT SUBSTITUTE

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON IMPLANT 500 CORALLINE HYDROXYPATITE BONE VOID FILLER (FORMERLY INTERPORE 500)

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEON IMPLANT 500 CORALLINE HYDROXYAPATITE BONE VOID FILLER

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·PRO OSTEON IMPLANT 500 POROUS HYDROXYAPATITE BONE GRAFT SUBSTITUTE BLOCKS & GRANULES

    Filler, Bone Void, Non-Osteoinduction

    FDA Pre-Market Approval
    FDA Class 3 ·INTERPORE PRO OSTEAN(R)IMPLANT 500 COR. HYDROX

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88600051·Max. 2. Molar band W-Fit left 05

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707031871·WEB 1ST MOLAR BANDS n.LR 5

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989051469·UPPER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 5

    Sternum Retractor

    FDA UDI
    KOROS U.S.A., INC.·10840199536075·Neonatal Sternum Retractor Double Blades 11mm Deep

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88600050051·Max. 2. Molar band W-Fit left 05

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88600050101·Max. 2. Molar band W-Fit left 05

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88600050501·Max. 2. Molar band W-Fit left 05

    SureLOK MIS 3L

    FDA UDI
    PRECISION SPINE, INC.·00840019920285·Caddy, CL Curved Rod Titanium