18 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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VIALOK SINGLE VIAL ACCESS DEVICE VENTED
FDA 510(k)
FDA Class 2
·General Hospital
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X1222650·12mm H x 22mm W x 65mm L x 0 degrees XLIF
CORNEAL TREPHINE HANDLE
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896072626·CORNEAL TREPHINE HANDLE
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X12226580·12mm H x 22mm W x 65mm L x 8 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587X122265120·12mm H x 22mm W x 65mm L x 12 degrees XLIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587L122265120·12mm H x 22mm W x 65mm L XLIF Trial 12 degree L...
NA
FDA UDI
aap Implantate AG·04042409089008·APS Lag Screw, self-tapping, TL 22, L 65
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970478·
ONE TOUCH PROFILE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·April 22, 2002
LINEAR ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 19, 2023
LDR SPINE USA C-PLATE, TL ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LIGHT TIP
FDA 510(k)
FDA Class 2
·Dental
NA
FDA UDI
aap Implantate AG·04042409089015·APS Lag Screw, self-tapping, TL 22, L 65
ARCHITECT CYCLOSPORINE
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code MKW·November 14, 2016
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·May 21, 2013
TITANIUM HEXALOBE SET SCREW
FDA Adverse Event
Malfunction
·ALPHATEC SPINE INC·Product code KWP·June 13, 2011
LIGASURE ATLAS HANDSWITCHING 20 CM
FDA Adverse Event
Malfunction
·COVIDIEN LP (US SURGICAL)·Product code GEI·August 12, 2008
Alligator Retrieval Device The device is intended for use in the peripheral and neurovasculature for foreign body removal. Catalog No. FA-88810-20V04 FA-88810-20V06 FA-88810-30V04 FA-88810-30V06 FA-88810-40V04 FA-88810-40V06 FA-88810-50V04 FA-88810-50V06
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·November 16, 2016