14 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CEREC Cercon 4D Abutment Blocks, CEREC Cercon 4D Abutment System
FDA 510(k)
FDA Class 2
·Dental
Sonoma™
FDA UDI
Seaspine Orthopedics Corporation·10889981051563·Bone Screw, Variable, Double Lead, 4.0 x 18mm
Insignia
FDA UDI
ALPHATEC SPINE, INC.·00190376266657·4.0mm Fixed Angle, Self Tapping Screw, Dual Lea...
Manta Ray™
FDA UDI
Seaspine Orthopedics Corporation·10889981057558·Screw - Self-Tapping - Variable - 4.0x18 mm
M.U.S.T. PEDICLE SCREWS SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
Yomi Robotic System
FDA 510(k)
FDA Class 2
·Dental
Mighty Wire Guide Wire
FDA 510(k)
FDA Class 2
·Cardiovascular
M.U.S.T. PEDICLE SCREW SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·January 13, 2026
GUIDE WIRE CAGE
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·January 18, 2012
M.U.S.T. PEDICLE SCREWS SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2014
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 6, 2011
BOLERO
FDA Adverse Event
Malfunction
·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·July 11, 2013
M.U.S.T. SACRAL ILIAC SCREW AND PELVIC TRAUMA SYSTEM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code OUR·October 16, 2024