30 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00
FDA 510(k)
FDA Class 2
·Orthopedic
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567289·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567319·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567272·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567296·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567326·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567258·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567302·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033567265·
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011014154000·Ligature cutter
SPINE SCOPE, MODEL 2180
FDA 510(k)
FDA Class 2
·Orthopedic
ELIPAR FREELIGHT
FDA 510(k)
FDA Class 2
·Dental
NA
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·March 7, 2012
OT PING ENHANCED METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 21, 2013
TENDRIL SDX
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·March 10, 2011
ICY HOT HEAT THERAPY PATCH
FDA Adverse Event
Other
·CHATTEM, INC.·Product code IMD·March 13, 2008
Facial Plastic Pack, part number AMS3327(C
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017
VACUETTE BLOOD COLLECTION TUBE 3ML K2E K2EDTA
FDA Adverse Event
Malfunction
·GREINER BIO-ONE NA INC.·Product code JKA·November 2, 2020
THERASPHERE
FDA Adverse Event
Death
·BIOCOMPATIBLES UK LTD·Product code NAW·August 24, 2017
UNK - CONSTRUCTS: PFN
FDA Adverse Event
Injury
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HSB·February 14, 2020