9 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DISPOSABLE BIPOLAR TEMPORARY PACING ELECTRODE
FDA 510(k)
FDA Class 2
·Cardiovascular
GC Initial™
FDA UDI
Gc America Inc.·15400556707439·GC Initial™ Zr-FS Dentin DB4, 20g
GC Initial™
FDA UDI
Gc America Inc.·J0228750591·GC Initial™ Zr-FS Dentin DB4, 20g
I.V. SET W/SINGLE-CHANNEL CASSETTE
FDA 510(k)
FDA Class 2
·General Hospital
AUDIANT BONE CONDUCTOR OR A.B.C.
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
2.5MM DHS/DCS GUIDE WIRE W/THREADED TIP 230MM
FDA Adverse Event
Malfunction
·SYNTHES BALSTHAL·Product code LRN·June 16, 2014
TI PANGEA LOCKING CAP
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code NKB·October 14, 2010
4.5MM TI CANCELLOUS POLYAXIAL SCREW 36MM FOR 4.0MM RODS
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code NKB·December 17, 2012
SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037
FDA Enforcement
Class II
·Completed·Townsend Design·January 17, 2024