7 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NATURAL-KNEE II SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OPTICON(TM) CONNECTOR ADAPTER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
3 LEAD CONNECTOR
FDA 510(k)
FDA Class 2
·General Hospital
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·October 21, 2020
REJUVENATE STRGHT PRFIT TMZF MOD STEM SIZE 9
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS-MAHWAH·Product code MEH·January 30, 2013
UNK
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code EZW·December 14, 2010
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 15, 2014