10 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APTUS Foot System 2.8-3.5
FDA 510(k)
FDA Class 2
·Orthopedic
Bernafon
FDA UDI
Sbo Hearing A/S·05714464033379·BERNAFON CROS MNR T R MSIL
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112748·BARRON VACUUM PUNCH 7.25MM
Sklar®
FDA UDI
SKLAR CORPORATION·10649111288357·SKLARLITE HALSTED MOSQ STR 5"
N/A
FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369665·THOMAS LEG SPLINT RADIOLUCENT EXTRA WIDE
ENDOHELIX ENDARTERECTOMY DEVICE
FDA 510(k)
FDA Class 2
·Cardiovascular
PERCLOT TOPICAL
FDA 510(k)
FDA Unclassified
·Unknown
VIGILANCE II CONTINUOUS CARDIAC OUTPUT COMPUTER
FDA Adverse Event
Malfunction
·EDWARDS LIFESCINECES·Product code DXG·November 3, 2008
ASR UNI FEMORAL IMPL SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·September 1, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 17, 2013