95 results · 30ms · 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.

Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

FDA Pre-Market Approval
FDA Class 3 ·CONSERVE PLUS TOTAL RESURFACING HIP SYSTEM

Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

FDA Pre-Market Approval
FDA Class 3 ·CONSERVE PLUS TOTAL RESURFACING HIP SYSTEM

Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

FDA Pre-Market Approval
FDA Class 3 ·CONSERVE PLUS HIP RESURFACING SYSTEM NEW ENROLLMENT STUDY (NES) PROTOCOL

Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

FDA Pre-Market Approval
FDA Class 3 ·CONSERVE PLUS TOTAL RESURFACING SYSTEM

ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

FDA UDI
FX SOLUTIONS·03701037308998·HUMELOCK REVERSED GLENOSPHERE CLAMP SUPERIOR L...

SCFE Screw

FDA UDI
ORTHOPEDIATRICS CORP.·00841132114209·4.0mm X 42mm MED THREAD CANNULATED SCREW

B-P TOTAL HIP SYSTEM

FDA UDI
ENDOTEC, INC.·00814193023049·B-P HIP FEMORAL RESURFACING CUP W/BIOCOAT & W/U...

uNion MAX

FDA UDI
Ulrich Medical Usa, Inc.·00810076334639·High Angulation Plate, 3-Level, 42 mm

SYNOVO HIP COMPONENTS

FDA UDI
Synovo Production·00814193025708·HIP FEMORAL RESURFACING CUP - 42.5MM

NA

FDA UDI
STRYKER CORPORATION·04546540756541·UNIVERSAL WEDGE 7MM X 30MM (1.5MM BORE)

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710410300420·Anterior Closing Wedge Osteotomy Guide, 30mm x ...

Intelliguides

FDA UDI
Mios Marketing, LLC·G2710420300420·Anterio Lateral Closing Wedge Osteotomy Guide, ...

PREMIER III PHASED ARRAY CTL SPINE COIL

FDA 510(k)
FDA Class 2 ·Radiology

Ambassador

FDA UDI
Choice Spine, LP·10885862269195·

R3 36MM ID US CRMC LINER 54

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code JDH·December 2, 2015

FDA Pre-Market Approval
IMAGECHECKER CT CAD SOFTWARE SYSTEM

Lens, Intraocular, Accommodative

FDA Pre-Market Approval
FDA Class 3 ·CRYSTALENS MODEL AT-45 ACCOMMODATING POSTERIOR CHAMBER INTRAOCULAR LENS (IOL)

ALINITY I ANTI-HCV REAGENT KIT

FDA Adverse Event
Malfunction ·ABBOTT GMBH·Product code MZO·April 30, 2026

Lens, Intraocular, Accommodative

FDA Pre-Market Approval
FDA Class 3 ·CRYSTALENS MODEL AT-45 ACCOMMODATING INTRAOCULAR (IOL)

Lens, Intraocular, Toric Optics

FDA Pre-Market Approval
FDA Class 3 ·TRULIGN TORIC POSTER CHAMBER INTRAOCULAR LENS