127 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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AFT
FDA 510(k)
FDA Class 2
·Orthopedic
HairCheck-DT (Opiates)
FDA UDI
Quest Diagnostics·00868586000223·HairCheck-DT (Opiates) is an ELISA test kit use...
Flex
FDA UDI
Diversified Products, Inc.·00037741504214·
Arthrex®
FDA UDI
ARTHREX, INC.·00888867522725·Cannulated Canc Screw, FT, 7.0x125mm
AOS CANNULATED CANCELLOUS SCREW, FULLY THREADED 7.0mm x 125mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665010367·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690192893·12mm X 150mm Stem Pilot
Flex
FDA UDI
Diversified Products, Inc.·00842894114810·
Flex
FDA UDI
Diversified Products, Inc.·00842894122792·
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 10, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019
PINS AND WIRES
FDA 510(k)
FDA Class 2
·Orthopedic
OPUS MAGNUM ANCHOR & INSERTER
FDA 510(k)
FDA Class 2
·Orthopedic
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Death
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 4, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 8, 2019