17 results · 30ms · Sources: EU EUDAMED, US FDA

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OPTIBOND

FDA 510(k)
FDA Class 2 ·Dental

ReLine

FDA UDI
Nuvasive, Inc.·00195377069979·RELINE C Screw, 3.5x46mm FA Part Thread

ZAVATION

FDA UDI
Zavation LLC·00842166191600·Reduction Shaft Screw 3.5x46

MAXIM ACCEL KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

3M ATTEST(TM) AUTO-READER

FDA 510(k)
FDA Class 2 ·General Hospital

PERFORMANCE TOTAL KNEE PROSTHESIS

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code HRY·October 25, 2019

PERFORMANCE DISTAL FAB LM/RL MED

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

PERFORMANCE DISTAL FAB LL/RM MED

FDA Adverse Event
Injury ·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016

VANGRD CR POR/HA FEM - RT 72.5

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

TINBN VNGRD INT CR ANAT FEMORAL R 62.5 MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 31, 2016

VANGUARD CR POROUS/HA FEM - RT 72.5

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·March 23, 2016

MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT

FDA Adverse Event
C.T.M. HOMECARE PRODUCT, INC·Product code INI·January 22, 2013

SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INRAOCULA

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·December 1, 2010

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE REHABILITATION EQUIP·Product code CAW·July 9, 2014

VANGUARD CEMENTLESS POROUS CR FEMORAL LT 65

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·April 20, 2017

VANGUARD CRUCIATE RETAINING POROUS HA FEMUR - RIGHT 65 MM

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·May 12, 2017

1.85MM TI MATRIX SCREW SELF-TAPPING/4MM

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code JEY·January 21, 2015