103 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Quantium
FDA 510(k)
FDA Class 2
·Dental
LCP
FDA UDI
Synthes GmbH·10886982168948·4.5MM LCP® PROXIMAL FEMUR PLATE 16 HOLES/391MM-...
EBI, LLC
FDA registration
EBI, LLC·2 products·🇺🇸 United States
C-TEK MAXAN
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWQ·May 20, 2011
ARRAY IMPLANTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWP·July 27, 2011
ARRAY IMPLANTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWP·July 27, 2011
ARRAY IMPLANTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWP·July 27, 2011
POLARIS SPINAL SYSTEM
FDA Adverse Event
Injury
·EBI, LLC.·Product code NKB·July 1, 2015
HELICAL FLANGE PLUG
FDA Adverse Event
Injury
·EBI, LLC.·Product code KWP·October 16, 2015
POLARIS 6.35/SYNERGY SPINAL SYSTEM IMPLANTS AND INSTRUMENTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWQ·September 1, 2011
POLARIS 6.35/SYNERGY SPINAL SYSTEM IMPLANTS AND INSTRUMENTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWQ·September 1, 2011
POLARIS 6.35/SYNERGY SPINAL SYSTEM IMPLANTS AND INSTRUMENTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWQ·September 1, 2011
ZYSTON CURVE SPACER SYSTEM AND INSTRUMENTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code MAX·September 27, 2011
ZYSTON CURVE SPACER SYSTEM AND INSTRUMENTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code MAX·September 27, 2011
ZYSTON CURVE SPACER SYSTEM AND INSTRUMENTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code MAX·September 27, 2011
POLARIS 5.5 SYSTEM IMPLANTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code NKB·August 29, 2011
POLARIS 5.5 SYSTEM IMPLANTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWQ·August 29, 2011
POLARIS 5.5 SYSTEM IMPLANTS
FDA Adverse Event
Malfunction
·EBI, LLC·Product code KWQ·August 29, 2011
SPF MINI
FDA Adverse Event
Malfunction
·EBI, LLC·Product code LOE·August 29, 2011
TRAUMACAD 1.2
FDA 510(k)
FDA Class 2
·Radiology