7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PROGRAMMABLE STIMULATOR 2352
FDA 510(k)
FDA Class 2
·Cardiovascular
STRAUMANN MAGELLAN(TM) ABUTMENT,PROTECTIVE CAP,TITANIUM COPINGS,GOLD CHOPINGS,BASAL SCREW
FDA 510(k)
FDA Class 2
·Dental
ERBE BICLAMP OPEN AND LAPAROSCOPIC INSTRUMENTS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
UNKNOWN URETEX MESH PRODUCT
FDA Adverse Event
Injury
·SOFRADIM PRODUCTION·Product code OTN·May 19, 2014
SOLYX SIS SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·November 15, 2012
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·September 9, 2010
KANGAROO
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code KNT·June 12, 2024