27 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REPOSABLE INSTRUMENT SYSTEM, MODELS MF001-MF083
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0142090·Trial, TLIF, 32L OB CRV 7Deg, 9mm
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0142080·Trial, TLIF, 32L OB CRV 7Deg, 8mm
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033576021·
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0102070·Shaver, Open 7mm
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571811·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571804·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571873·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571842·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571866·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571828·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571859·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033571835·
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0112070·Tap, Cannulated, 5.5 mm
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345023901·PADDLE SPREADER, 7MM
LASER PERIPHERALS REUSABLE HOLMIUM FIBER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PORTABLE INSTENSIVE CARE UNIT
FDA 510(k)
FDA Class 3
·Cardiovascular
ZPower Rechargeable System for Hearing Aids
FDA UDI
ZPOWER, LLC·00811204030119·Contains Charger (00811204030164) and two batte...
PIPELINE EMBOLIZATION DEVICE
FDA Adverse Event
Death
·EV3 NEUROVASCULAR·Product code OUT·June 24, 2014
ENDEAVOR SPRINT RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·March 21, 2013