9 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MOUNTABLE ENDOSCOPIC BLADE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450179673·
MENICON Z
FDA 510(k)
FDA Class 2
·Ophthalmic
VERSALUX
FDA 510(k)
FDA Class 2
·Dental
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·January 29, 2026
DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·April 26, 2013
INTEGRIS ALLURA 15-12 (MONO)
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code IZI·April 7, 2011
UNKNOWN DEPUY UNI TIBIAL
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HSH·July 18, 2008
On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in relation to anatomical and fiducial landmarks.
FDA Enforcement
Class II
·Terminated·Varian Medical Systems, Inc.·April 30, 2014