10 results
·
26ms
·
Sources: EU EUDAMED, US FDA
BANDAGE, WRINKY-LASTIC ELASTIC GAUZE
FDA 510(k)
FDA Class 1
·General Hospital
ILIF
FDA UDI
Nuvasive, Inc.·00887517263322·ILIF Inserter, Tanged
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668110546·QUICK SWITCH IRRIGAT-ASPIRAT HAND PIECE
Inertia® CONNEXX™ Modular Pedicle Screw System
FDA UDI
NEXXT SPINE, LLC·00889929046883·Straight Rod, Ø6.0x140 mm
CRP-ADVANCE MULTI CALIBRATOR SET, MODEL SE-250
FDA 510(k)
FDA Class 2
·Clinical Chemistry
DENTRIa series
FDA 510(k)
FDA Class 2
·Radiology
ACCESS
FDA Adverse Event
Malfunction
·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·April 18, 2014
ASR 300 SPIKED CUP SIZE 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·September 26, 2012
PRECISION XTRA
FDA Adverse Event
Injury
·Product code NBW·July 16, 2010
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 125 MM, Silicone, Sterile, Item 431190.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020