7 results
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18ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STAPLE, FIXATION BONE; SCREW FIXATION BONE
FDA 510(k)
FDA Class 2
·Orthopedic
OSTEOMED SUBTALAR IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
UGFT3; FHT7
FDA 510(k)
FDA Class 2
·General Hospital
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTP·January 28, 2013
VISISTAT SKIN STAPLER
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code GDT·November 15, 2010
ENDEAVOR SPRINT RX
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIQ·July 14, 2014
Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026