Tribio® DP Evans Wedge

FDA UDI

BERKELEY ADVANCED BIOMATERIALS, LLC·00816125023769·Tribio® DP Wedge is a bone void filler consisti...

RABEA 0°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000588·The basic shape of the NUBIC and RABEA devices ...

RABEA 5°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000151·The basic shape of the NUBIC and RABEA devices ...

RABEA 5°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844014059·The basic shape of the NUBIC and RABEA devices ...

RABEA 5°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000366·The basic shape of the NUBIC and RABEA devices ...

RABEA 0°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000472·The basic shape of the NUBIC and RABEA devices ...

NUBIC

FDA UDI

SIGNUS Medizintechnik GmbH·04047844010532·The basic shape of the NUBIC and RABEA devices ...

RABEA 5°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000342·The basic shape of the NUBIC and RABEA devices ...

RABEA 0°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000519·The basic shape of the NUBIC and RABEA devices ...

RABEA 5°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000601·The basic shape of the NUBIC and RABEA devices ...

RABEA 0°

FDA UDI

SIGNUS Medizintechnik GmbH·04047844000250·The basic shape of the NUBIC and RABEA devices ...

SpaceFlex Shoulder

FDA UDI

G21 SRL·08058964726049·Disposable cement spacer molds with metal reinf...

SpaceFlex Shoulder

FDA UDI

G21 SRL·08058964724977·Disposable cement spacer molds with metal reinf...

SpaceFlex Shoulder

FDA UDI

G21 SRL·08058964726087·"Disposable cement spacer molds with metal rein...

SpaceFlex Shoulder

FDA UDI

G21 SRL·08058964726056·Disposable cement spacer molds with metal reinf...

SpaceFlex Shoulder

FDA UDI

G21 SRL·08058964726070·Disposable cement spacer molds with metal reinf...

SpaceFlex Shoulder

FDA UDI

G21 SRL·08058964726063·Disposable cement spacer molds with metal reinf...

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval

FDA Class 3 ·Senza HFX iQ System, Senza HFX iQ IPG, HFX Trial Stimulator, HFX iQ Remote, HFX iQ Patient Application

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval

FDA Class 3 ·MEDTRONIC MODEL 7278 MAXIMO DR ICD AND MODEL 7232 MAXIMO VR ICD SYSTEMS, WITH MODEL 9978 VERSION 1.0 APPLICATION SOFTWA

Intraocular Lens

FDA Pre-Market Approval

FDA Class 3 ·HYDROVIEW IOLS