10 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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INTERMEDULLARY BRUSH
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
NA
FDA UDI
KEY SURGICAL, INC.·00849771048220·K-Wire and Steinmann Pin Dispensers, .062-inch...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292336·DISP K-WIRE FOR .062" (1.6MM) 12.25"
K-Wire and Steinmann Pin Dispensers
FDA UDI
KEY SURGICAL, INC.·00849771012054·K-Wire and Steinmann Pin Dispensers, .062-inch...
Welch Allyn, Inc.
FDA UDI
WELCH ALLYN, INC.·00732094150421·Welch Allyn Green Series 777 Wall Diagnostic Sy...
DEPUY RESTORE ORTHOBIOLOGIC SOFT TISSUE IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PACING KIT, ELECATH TRANSTHORACIC
FDA 510(k)
FDA Class 2
·Cardiovascular
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 25, 2007
HI-TORQUE VERSACORE MODIFIED J GUIDE WIRE SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code DQX·October 3, 2012
MONARCH IOL DELIVERY SYSTEM HANDPIECE - UNK
FDA Adverse Event
Injury
·ALCON PRECISION DEVICE - SINGKING SPRING·Product code HQL·December 18, 2013