32 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATION TO: 1.5 BONE FIXATION KIT, MODELS BXS6114, BXS6214
FDA 510(k)
FDA Class 2
·Orthopedic
ACUFEX
FDA UDI
Smith & Nephew, Inc.·03596010091031·10 MM CANNULATED DRILL BIT
CARDINAL HEALTH
FDA UDI
Cardinal Health 200, LLC·10887488023625·IV START KIT
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584620·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584590·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584606·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584583·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584637·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033584613·
Phantom® Fibula Nail System
FDA UDI
Paragon 28, Inc.·00889795134226·3.5mm x 46mm, Threaded Peg, Ti
VenSure Nav Balloon Dilation System
FDA UDI
Fiagon GmbH·04260759931260·Balloon Dilation system as set including navi...
POWDER FREE LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
OPTIMA URS UNIVERSAL RADIOGRAPHIC SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
PERFORMANCE TOTAL KNEE PROSTHESIS
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code HRY·October 25, 2019
ACCU-CHEK ® COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·December 9, 2013
PERFORMANCE DISTAL FAB LM/RL MED
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016
PERFORMANCE DISTAL FAB LL/RM MED
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·October 18, 2016
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 11, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 11, 2025
INSET II
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 11, 2025