16 results · 47ms · 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.

HARMONIC ACE 36 CM

FDA Adverse Event
Injury ·ETHICON ENDO SURGERY, INC.·Product code LFL·December 12, 2005

VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 71/75 X 14MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 71/75X14MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

ENTERRA

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·April 9, 2013

ICL (IMPLANTABLE COLLAMER LENS)

FDA Adverse Event
Injury ·STAAR SURGICAL COMPANY·Product code HQL·April 6, 2011

ENDOTAK ENDURANCE RX

FDA Adverse Event
Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008

VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING 63/67X14MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 7, 2016

VANGUARD DA 360 TIBIAL BEARING ARCM 71/75X16

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·April 28, 2017

VANGUARD DUAL ARTICULATING (DA) BEARING 71/75 X 16 MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·February 6, 2017

VG DA360 TIB BRG ARCM 79/83X14 3 X 14MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDG·October 31, 2017

VANGUARD DA 360 KNEE SYSTEM ARCOM TIBIAL BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 2, 2017

VANGUARD DUAL ARTICULATING (DA) BEARING 71/75 X 16 MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·October 13, 2016

VANGUARD DA 360 TIBIAL TRAY

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·April 27, 2017

VANGUARD SSKPSC TIBIAL BEARING S 12X63/67

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·July 21, 2017

VANGUARD DA360 TIBIAL BEARING ARCOM 63/67X18

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 9, 2017

WARMER DRAPE

FDA Adverse Event
Malfunction ·MICROTEK DOMINICANA, S.A.·Product code LHC·February 26, 2016