27 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LIFESIGN COC, STATUS STIK COC, ACCUSIGN STIK COC, ACCUSTIK COC
FDA 510(k)
FDA Class 2
·Clinical Toxicology
InTess C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07309K01406T0·Cervical Rasp, 15 x 12, 6mm, 7 Degree, Tapered
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558881·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558867·
InTess C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07309K01406N0·Cervical Rasp, 15 x 12, 6mm, 0 Degree, No Taper
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558874·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033575024·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033558850·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033575031·
CONTACT DETACH
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 29, 2026
ASEPTIC BATTERY HOUSING
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL SA·Product code MOQ·June 30, 2021
ASEPTIC BATTERY HOUSING
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL SA·Product code MOQ·June 30, 2021
ASEPTIC BATTERY HOUSING
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL SA·Product code MOQ·June 30, 2021
ASEPTIC BATTERY HOUSING
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL SA·Product code MOQ·June 30, 2021
ASEPTIC BATTERY HOUSING
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL SA·Product code MOQ·June 30, 2021
ASEPTIC BATTERY HOUSING
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL SA·Product code MOQ·June 30, 2021
Clever Choice
FDA UDI
SIMPLE DIAGNOSTICS INC·00898302140698·Replacement Cuff for Automatic Blood Pressure M...
DURABOND NON-PRECIOUS CERAMIC ALLOY
FDA 510(k)
FDA Class 2
·Dental
AQUASENS FLUID MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
HEARTSINE SAMARITAN 300P AND PAD-PAK K014067
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES LTD·Product code MKJ·July 19, 2018