12 results
·
28ms
·
Sources: EU EUDAMED, US FDA
MODIFIED AMANA ELECTROTHERAPEUTIC SYSTEM
FDA 510(k)
FDA Class 2
·Neurology
SA Repl. Med. Cvr. 25x30mm (4 Hr) 5-Pk, Velashape III
FDA UDI
Candela Corporation·00817495024561·SA Repl. Med. Cvr. 25x30mm (4 Hr), Velashape III
GC Initial™
FDA UDI
Gc America Inc.·J0228750721·GC Initial™ Zr-FS Translucent TN, 20g
GC Initial™
FDA UDI
Gc America Inc.·15400556708870·GC Initial™ Zr-FS Translucent TN, 20g
ARROW XT POWERED WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
MAXIMUS CUSHION
FDA 510(k)
FDA Class 1
·Physical Medicine
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·May 30, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·May 30, 2024
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·May 30, 2024
ACCENT DR RF
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·June 16, 2014
INSYNC III
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·October 19, 2010
UNKNOWN DEPUY LCS 10MM TIB INSERT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·December 17, 2012