63 results · 23ms · Sources: EU EUDAMED, US FDA

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Luna 3D GEN2 Interbody Fusion System

FDA 510(k)
FDA Class 2 ·Orthopedic

Vanguard® Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304271616·

UNIVERSAL SURGERY TRAY

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896019577·UNIVERSAL SURGERY TRAY WITH LID KEYHOLE BRACKETS

Vanguard Knee System

FDA UDI
Biomet Orthopedics, LLC·00880304473232·

Avalign

FDA UDI
Avalign Technologies, Inc.·00190776022884·Surgical Case

EXPANDED SPECTRUM PHOTO THERAPY DEVICE, MODEL ESPT-3X

FDA 510(k)
FDA Class 2 ·Physical Medicine

SHASER IPL HAIR REMOVAL SYSTEM

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

VANGUARD CR ILOK FEM-LT 75

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OYC·October 18, 2014

POSSIS

FDA Adverse Event
Injury ·EXTERNAL MANUFACTURER·Product code NHW·July 29, 2011

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013

VANGUARD CR ILOK FEM-LT 70

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2018

VANGUARD CR ILOK FEM-LT 70

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

VANGUARD CR ILOK FEM-LT 75

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2018

VANGUARD COMPLETE KNEE SYSTEM - CRUICIATE RETAINING INTERLOK FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

VANGUARD CR ILOK FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

VANGUARD CR ILOK FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

BIOMET CC I-BEAM TIBIAL TRAY

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

VANGUARD COMPLETE KNEE SYSTEM - CRUICIATE RETAINING INTERLOK FEMORAL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

UNKNOWN PATELLA

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018