7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CEFOTETAN 30 MCG SENSI DISC
FDA 510(k)
FDA Class 2
·Microbiology
Chaorum Implant System
FDA 510(k)
FDA Class 2
·Dental
OSTEOMED 1ST MPJ HEMI IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
CAPSURE SENSE
FDA Adverse Event
Injury
·MPRI·Product code DTB·June 10, 2014
FINELINE II
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 7, 2010
PULSE GEN MODEL 102
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·December 6, 2012
OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.
FDA Enforcement
Class I
·Terminated·GE OEC Medical Systems, Inc·August 1, 2012