28 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KI-20
FDA 510(k)
FDA Class 1
·Dental
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304011045·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868230769·
SONICATOR PLUS 920
FDA 510(k)
FDA Class 2
·Physical Medicine
EM-9000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
WAVEWRITER ALPHA 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 24, 2024
VERSAFITCUP CC TRIO CEMENTLESS CUP 48
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL, SA·Product code LZO·October 1, 2014
VANGUARD PS TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017
BIOMET OFFSET TIBIAL TRAY ADAPTOR
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBV·November 29, 2017
BIOMET SMOOTH KNEE STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 29, 2017
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·June 1, 2011
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·October 4, 2014
RHK CEMENTED STEM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·March 6, 2019
RHK CEMENTED STEM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·March 6, 2019
AGC MODULAR POST SCREW
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·March 6, 2019
VANGUARD PS OPEN FEMORAL INTERLOCK
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·October 18, 2017
BIOMET OFFSET TIBIAL TRAY ADAPTOR
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code JWH·March 6, 2019
VNGD SSK PSC TIB BRG 18X63/67
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·September 14, 2017
RHK 12X80 CEMENTED STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JWH·April 9, 2019