21 results · 23ms · Sources: EU EUDAMED, 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