308 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Preference Elite Pedicle Screw System
FDA 510(k)
FDA Class 2
·Orthopedic
Oticon
FDA UDI
Oticon A/S·05707131327390·OPN 1 FW 1
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141172·ZEUS® LLIF 16mm x 21mm x 60mm x 14° TRIAL
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916120542·ZEUS®-L Hyper, 16 x 21 x 60mm, 14 Degree
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141226·ZEUS® LLIF 16mm x 21mm x 60mm x 28° TRIAL
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141202·ZEUS® LLIF 16mm x 21mm x 60mm x 21° TRIAL
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916141134·ZEUS® LLIF 16mm x 21mm x 60mm x 07° TRIAL
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916134396·ZEUS®-L, Lateral Lumber Interbody Fusion Device...
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916120559·ZEUS®-L Hyper, 16 x 21 x 60mm, 21 Degree
ZEUS-L
FDA UDI
SPINAL ELEMENTS·00840916134365·ZEUS®-L, Lateral Lumber Interbody Fusion Device...
STRETCH VINYL EXAMINATION GLOVE POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
GO GO MINI, MODEL SC30
FDA 510(k)
FDA Class 2
·Physical Medicine
IMP TM 4.7MM MTX FULL, 11.5MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·November 25, 2022
IMP TM 4.7MM MTX FULL, 10
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026
IMP TM 4.7MM MTX FULL, 10
FDA Adverse Event
Injury
·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 10, 2014
ENGINE DRIVEN HEDSTROEM FILE
FDA Adverse Event
Injury
·DENTSPLY TULSA DENTAL SPECIALTIES·Product code EKS·July 7, 2011
7900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 6, 2013
IMP TM 4.1MM MTX FULL, 11.5MM
FDA Adverse Event
Injury
·ZIMMER DENTAL·Product code DZE·June 1, 2020
DUETTO MT
FDA Adverse Event
Malfunction
·QUANTA SYSTEM S.P.A.·Product code GEX·April 14, 2022