103 results · 27ms · Sources: EU EUDAMED, 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