46 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
POINT 4 MODIFIED
FDA 510(k)
FDA Class 2
·Dental
NA
FDA UDI
Stryker GmbH·00886385005294·Cortical Screw, Self-tap., T10 Drive
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033506233·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033506219·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033506226·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033506240·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00192304138982·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00192304138999·
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033506202·
General Instruments
FDA UDI
ALPHATEC SPINE, INC.·00811801031663·Bayoneted Nerve Root Retractor w/ Lip 10mm
SOFIA VERGARA
FDA UDI
FGX INTERNATIONAL INC.·00193033506257·
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345027237·Inserter, 7-10MM, Lumbar Straight
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0131100·Assembly, Rod Inserter, Fixed UNID
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K0131100·Rocker, One Piece
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130100·Segmental Rod Reducer Assembly
INSTATRAK SYSTEM WITH FLUOROCAT, MODEL IT3500
FDA 510(k)
FDA Class 2
·Radiology
BALLOON CANNULA, SHORT, MODEL R65-985; BALLOON CANNULA, LONG, MODEL R65-985-1
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
IPC® HANDPIECE - INDIGO¿ DRILL
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code HBE·October 3, 2017
BREEZE2
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·February 18, 2015
CONTOUR
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE LLC·Product code NBW·April 29, 2014