7 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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XOMED FEATHERTOUCH XPS POWER RASP ATTACHMENT
FDA 510(k)
FDA Class 2
·Orthopedic
Polystar Selection EDITION HD
FDA UDI
Merz Dental GmbH·D7091983025·posteriors; shade A3.5; size XL; lower jaw
MOBIO Total Knee System Posterior Stabilized (PS and PS+) Tibial Inserts, MOBIO Total Knee System Patellar Component
FDA 510(k)
FDA Class 2
·Orthopedic
SYNTHES 4.5 MM VA-LCP CURVED CONDYLAR SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code MMH·February 28, 2013
EXTERNAL STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LGW·February 4, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 6, 2014