9 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OP3/VP4
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
APEX Revision Knee
FDA UDI
Omni Life Science, Inc.·00841690114284·PS-R Insert, Size 5 x 16mm
Solstice Occipito-Cervico-Thoracic System
FDA UDI
Life Spine, Inc.·00190837017132·
Duo Lumbar Interbody Fusion Device
FDA UDI
SPINEOLOGY INC.·M7402924516·Duo, Hyper-Lordotic, 45 x 16mm
GENERAL PURPOSE INSTRUMENT TRAY, STERILE, DISPOSAB
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
9 FRENCH LITHOTRIPTER ELECTRODE, MODIFICATION
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
5.0MM CANNULATED LOCKING SCREW70MM
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HRS·January 22, 2013
VIRTUOSO DR
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL, INC.·Product code LWS·December 14, 2010
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 9, 2014