10 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DERMA PRENE POWDER-FREE SYNTHETIC SURGICAL GLOVES (CHEMOTHERAPY USE)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984558·anteriors; shade C4; mould R 75
IOP ADJUSTABLE STIRRUP
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MINI LIGHTSCOPE SET, LIGHTSCOPE JR. SET
FDA 510(k)
FDA Class 2
·Orthopedic
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·April 22, 2022
PSO KNEE BONE SUBSTITUTION
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code KRO·July 18, 2019
PROMOTE Q CRT-D
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·February 28, 2013
ASR UNI FEMORAL IMPL SIZE 43
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 28, 2011
ACCU-CHEK ® AVIVA PLUS TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·August 6, 2014
UNKNOWN HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·February 16, 2018