16 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DEROYAL HYDROGEL DRESSING
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
3M BRAND EAR LOOP FACE MASK, 2000F
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OSCOR MEDICAL CORP. PERMANENT PACING PAD
FDA 510(k)
FDA Class 3
·Cardiovascular
PERFORMANCE MODULAR TIBIAL TRAY SML
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016
E1 HI-WALL LINER RINGLOC-X 60MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·January 10, 2017
PERFORMANCE FEMORAL STEM 16X100MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016
POLISHED IBEAM TIB TRAY 71MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·July 11, 2016
NON-POROUS PERF TIB TRAY-XSML
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·March 23, 2018
POLISHED FINNED TIBIAL TRAY 71 MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·March 10, 2017
POLISHED FINNED 1 PIECE TIBIAL TRAY
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·October 12, 2017
POLISHED FINNED TIBIAL TRAY 75MM
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·July 10, 2017
PLMA DVC V11.51 1 N
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·May 16, 2014
COBAS 6000 C501 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CKA·December 6, 2010
DEPUY ASR XL FEM IMP SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 15, 2013
MAXIM PRIMARY FEMORAL COMPONENT 75 MM LEFT / POROUS 75 LT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·October 30, 2017
DCM MAXIM PRIMARY TIBIAL BEARING 12 MM THICK X 71/75 WIDE ARCOM UHMWPE
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·October 30, 2017