111 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GS MEDICAL ANYPLUS PEEK LUMBAR CAGES (ALIF AND DLIF)
FDA 510(k)
FDA Class 2
·Orthopedic
Depth gauge
FDA UDI
Jeil Medical Corporation·08800089407736·
5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/65MM
FDA Adverse Event
Injury
·SYNTHES MEZZOVICO·Product code JDP·August 28, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 26, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·March 2, 2015
HIGH TIBIAL OSTEOTOMY PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FETCH 2 ASPIRATION CATHETER MODEL 109400-001
FDA 510(k)
FDA Class 2
·Cardiovascular
IMPLANT, FIXATION DEVICE CONDYLAR PLATE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code JDP·February 23, 2017
VALVE IN CARTRIDGE, 9MM
FDA Adverse Event
Injury
·Product code NJK·June 28, 2021
VALVE IN CARTRIDGE, 9MM
FDA Adverse Event
Injury
·Product code NJK·June 28, 2021
VALVE IN CARTRIDGE, 7MM
FDA Adverse Event
Injury
·Product code NJK·June 28, 2021
VALVE IN CARTRIDGE, 9MM
FDA Adverse Event
Injury
·GYRUS ACMI, INC·Product code NJK·May 21, 2022
VALVE IN CARTRIDGE, 7MM
FDA Adverse Event
Injury
·GYRUS ACMI, INC·Product code NJK·May 21, 2022
VALVE IN CARTRIDGE, 6MM
FDA Adverse Event
Injury
·GYRUS ACMI, INC.·Product code NJK·March 13, 2023
VALVE IN CARTRIDGE, 7MM
FDA Adverse Event
Injury
·GYRUS ACMI, INC.·Product code NJK·July 26, 2024
VALVE IN CARTRIDGE, 9MM
FDA Adverse Event
Injury
·GYRUS ACMI, INC.·Product code NJK·July 16, 2024
VALVE IN CARTRIDGE, 9MM
FDA Adverse Event
Injury
·Product code NJK·July 15, 2020
VALVE IN CARTRIDGE, 9MM
FDA Adverse Event
Injury
·Product code NJK·July 15, 2020
VALVE IN CARTRIDGE, 5MM
FDA Adverse Event
Injury
·Product code NJK·July 10, 2020
VALVE IN CARTRIDGE, 7MM
FDA Adverse Event
Injury
·Product code NJK·July 10, 2020