27 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Sonoma Fibula Repair System
FDA 510(k)
FDA Class 2
·Orthopedic
SMITH & NEPHEW, INC SPATIALFRAME V4.1 WEB-BASED SOFTWARE
FDA 510(k)
FDA Class 2
·Orthopedic
PALOMAR LUXIR FRACTIONAL HANDPIECE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Widex
FDA UDI
Widex A/S·05706069897579·WIDEX EVOKE E-FP (Summer gold ) 50, Telecoil, V...
Widex
FDA UDI
Widex A/S·05706069895889·WIDEX EVOKE E-FA (Summer gold ) 50, Telecoil, V...
Widex
FDA UDI
Widex A/S·05706069870602·WIDEX EVOKE E-FM (Summer gold ) 50, RC coil
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·June 10, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011
COLLEAGUE 3 VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·May 7, 2018
LARGE SET SCREW
FDA Adverse Event
Injury
·ORTHOPEDIATRICS, INC·Product code OSH·December 19, 2019
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017