34 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ORTHOPEDIC WIRE
FDA 510(k)
FDA Class 2
·Orthopedic
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776350604·SOPHER OVUM FCP
Zavation
FDA UDI
Zavation LLC·00842166108974·PLIF-C 11x27 Convex -14
Zavation
FDA UDI
Zavation LLC·00842166108929·PLIF-C 11x27 Convex -09
Zavation
FDA UDI
Zavation LLC·00842166108950·PLIF-C 11x27 Convex -12
Zavation
FDA UDI
Zavation LLC·00842166108981·PLIF-C 11x27 Convex -15
Zavation
FDA UDI
Zavation LLC·00842166108943·PLIF-C 11x27 Convex -11
Zavation
FDA UDI
Zavation LLC·00842166108936·PLIF-C 11x27 Convex -10
Zavation
FDA UDI
Zavation LLC·00842166108912·PLIF-C 11x27 Convex -8
Zavation
FDA UDI
Zavation LLC·00842166108998·PLIF-C 11x27 Convex -16
Zavation
FDA UDI
Zavation LLC·00842166108967·PLIF-C 11x27 Convex -13
Arlington PLIF Cage
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215026356·
Verteloc Lumbar Cage
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215129408·
DATEX-OHMEDA TEC 7 ANESTHESIA VAPORIZER (ENFLURANE)
FDA 510(k)
FDA Class 2
·Anesthesiology
ANCA COMBI DIAGNOSTIC KIT WITH IF-AIM TECHNOLOGY
FDA 510(k)
FDA Class 2
·Immunology
MOSAIC
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·March 12, 2019
HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DYE·May 27, 2020
LARGE SUTURECUT NEEDLE DRIVERINSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·November 7, 2013
SIG MOD TIB TRAY CEM COCR 3
FDA Adverse Event
Injury
·DEPUY (IRELAND) 9616671·Product code JWH·April 2, 2013
NEXGEN LCCK ARTICULAR SURFACE
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·March 22, 2011