8 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEOMARK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PIONEER SURGICAL TECHNOLOGY QUANTUM SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
GME LinScan Lite 808 Laser System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ARTICULEZE M HEAD 36MM +5 K980513
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·June 14, 2016
HEARTSTREAM FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 22, 2013
PRECISION TEST STRIPS
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE, INC. USA·Product code NBW·February 7, 2011
JAGWIRE?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - COSTA RICA (COYOL)·Product code EZB·August 5, 2014
PFNA-II BLADE L90 TAN
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HSB·October 8, 2018