8 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SURGIPEEL SELF-SEAL PACKAGING SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
PressON™
FDA UDI
NEXUS SPINE, L.L.C.·B6788203020·MIS XL Internal Retaining Driver
MECHANICAL WHEELCHAIR
FDA 510(k)
FDA Class 2
·Physical Medicine
Disposable surgical face mask
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HOYER
FDA Adverse Event
Malfunction
·SUNRISE MEDICAL·Product code FSA·May 15, 2014
UNKNOWN PRODUCT - XIA 2 TITANIUM ROD
FDA Adverse Event
Malfunction
·STRYKER SPINE BORDEAUX·Product code HSB·October 31, 2012
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code MDS·August 30, 2010
Lap-Band Access Port Needle 10-Pack, 20 G x 51 mm (2 in.), Product Code: 8-20302-10, Lot Number: 9L01N 20 gauge, 51 mm (2 in.) length non-coring deflected tip (Huber) needle, used with the LAP-BAND System for band adjustment.
FDA Recall
Terminated
·Allergan·Product code LTI·March 21, 2011