30 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SPLINE DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
Atos Medical Inc
FDA UDI
ATOS MEDICAL INC.·00817126020986·2010-073 Laryngectomy Pulmonary Kit with Standa...
TO BE ASSIGNED
FDA UDI
FGX INTERNATIONAL INC.·00193033380352·
TO BE ASSIGNED
FDA UDI
FGX INTERNATIONAL INC.·00193033380321·
TiWAVE C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07320K0100030·Implant Inserter, Cervical
TO BE ASSIGNED
FDA UDI
FGX INTERNATIONAL INC.·00193033380338·
InTess C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07309K0100030·Implant Inserter, InTess C
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100030·Tap, 4.5mm Cann, Chuckable
Ocata Anterior Cervical System
FDA UDI
Kalitec Direct LLC·B07308K0100030·Caddie Lid, Plates and Screws
TO BE ASSIGNED
FDA UDI
FGX INTERNATIONAL INC.·00193033380307·
TO BE ASSIGNED
FDA UDI
FGX INTERNATIONAL INC.·00193033380345·
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0100030·Caddie, 4 Level Plates
TO BE ASSIGNED
FDA UDI
FGX INTERNATIONAL INC.·00193033380314·
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100230·SNII Awl Tap, 7.50mm
Matira
FDA UDI
Kalitec Direct LLC·B07307K0100230·Assembly, Caddie, 4L Plates, Hinged
MERCURY MEDICAL DISPOSABLE RADIOFREQUENCY CANNULA
FDA 510(k)
FDA Class 2
·Neurology
EBI VUELOCK ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
BD PLASTIPAK 50ML CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·April 18, 2021
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013