33 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SYNTHES 3.9 MM PELVIC SCREWS
FDA 510(k)
FDA Class 2
·Orthopedic
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0130140·Sagittal Bender, Right
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033618455·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033618486·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033618479·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0100440·Assembly, Caddie, Locking Caps
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0100440·Caddie, Locking Caps
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033618615·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033618462·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130400·ROD REDUCER, AXIAL
COSMIC
FDA 510(k)
FDA Class 2
·Dental
COPELAND RESURFACING HEADS
FDA 510(k)
FDA Class 2
·Orthopedic
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
DISC LT DSTL HMRL BDY SET
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDC·April 1, 2019
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 17, 2017
UNKNOWN KUDO ELBOW
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDC·May 19, 2017