21 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO: RAINBOW ADHESIVE CO-OXIMETRY SENSORS
FDA 510(k)
FDA Class 2
·Cardiovascular
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704292398·
NA
FDA UDI
KEY SURGICAL, INC.·10849771048760·K-Wires, Double trocar, .054-inch (1.4mm) diame...
mahe medical GmbH
FDA UDI
mahe medical gmbh·04050659483941·K-Wire w. double end trocarpoint _x000D_...
BioQuick®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70710241·BioQuick-Brackets Roth .022" 5 cases Starter-as...
K-Wire w. double end trocarpoint 1.40mm/152mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM710240·K-Wire w. double end trocarpoint
1.40mm...
VIDASHIELD/UV24
FDA UDI
Medical Illumination International Inc.·00816835023882·Air Purifier with no light
Xsert Lumbar Expandable Interbody System
FDA UDI
Xtant Medical Holdings, Inc.·M697X0920710241·7mm-10mm x 10mm x 24mm PLIF ASSY
VIDASHIELD/UV24
FDA UDI
Medical Illumination International Inc.·00816835023875·Air Purifier with no light
LYNX
FDA UDI
HNM TOTAL RECON LLC·00841742111384·LYNX ø4.0mm Cancellous Screw, Full Thread, Ti -...
Xsert Lumbar Expandable Interbody System
FDA UDI
Xtant Medical Holdings, Inc.·M697X092071024STR1·7mm-10mm x 10mm x 24mm PLIF ASSY (Sterile)
WAVEWRITER ALPHA? 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·February 5, 2026
PASS SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CYBERKNIFE SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
LINEAR 3-4
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 22, 2023
UNICEL DXI 800 ACCESS® IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·August 4, 2011
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code DHA·August 17, 2011
SYNERGY
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·April 22, 2013
SIMPLEX P WITH TOBRA UNIT PACKFULL DOSE
FDA Adverse Event
Other
·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·April 20, 2011
ONE TOUCH ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code NBW·July 2, 2008