22 results · 25ms · 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.

ALIF Interfixated System

FDA 510(k)
FDA Class 2 ·Orthopedic

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704283068·RICHARDSON EASTMAN RETRACTOR 10 1/4" LARGE

DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169502154·INTERBODY 2151214 MEDIUM - 6 DEG 14MM

Pro Lift Instruments

FDA UDI
Life Spine, Inc.·00190837031244·

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291229·Knee femur prosthesis trial - Endo Model Knee S...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291243·Knee femur prosthesis trial - Endo Model Knee S...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291205·Knee femur prosthesis trial - Endo Model Knee S...

ATTUNE

FDA UDI
DEPUY (IRELAND)·10603295475163·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...

Endo-Model Knee System - Instruments

FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575291267·Knee femur prosthesis trial - Endo Model Knee S...

ATTUNE

FDA UDI
DEPUY (IRELAND)·10603295475156·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...

ATTUNE

FDA UDI
DEPUY (IRELAND)·10603295475187·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...

ATTUNE

FDA UDI
DEPUY (IRELAND)·10603295475170·ATTUNE KNEE SYSTEM REVISION CEMENTED STEM CEMEN...

ALUMA SKIN RENEWAL SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

GUARDIAN CONNECTION

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·November 18, 2020

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013

ARTICULEZE M HEAD 36MM -2

FDA Adverse Event
Malfunction ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code JDI·June 30, 2011

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORPORATION·Product code DZC·September 9, 2008

OT VERIO FLEX METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 1, 2015

ACCESS ACCUTNI REAGENT

FDA Adverse Event
Injury ·BECKMAN COULTER·Product code MMI·September 15, 2016