26 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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NON-INVASIVE VENTILATION NIV OPTION, MODEL 84 14 474
FDA 510(k)
FDA Class 2
·Anesthesiology
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00193033091395·
neoWave C
FDA UDI
XENIX MEDICAL LLC·00818345023833·Cervical Inserter
TiWAVE C Cervical Cage System
FDA UDI
Kalitec Direct LLC·B07320K0100030·Implant Inserter, Cervical
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
SIMPLY SPECS
FDA UDI
FGX INTERNATIONAL INC.·00193033091388·
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0100030·Caddie, 4 Level Plates
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
Navagio
FDA UDI
Kalitec Direct LLC·B073DRK0100330·Assembly, Navagio Fixed Draw Rod, Large Knob
CANDELA SPTL-1B PULSED DYE LASER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EBI VUELOCK ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
AXSYM DIGOXIN III
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013
ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·February 11, 2011
VUELOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020
VEULOCK SCREW, UNKNOWN SIZE
FDA Adverse Event
Injury
·ZIMMER BIOMET SPINE INC.·Product code KWQ·April 16, 2020