8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
BONE CURETTE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
FORZA
FDA UDI
Orthofix US LLC·18257200077250·8MM PADDLE DISTRACTOR
MTS Gentamicin 0.016 - 256 µg/mL
FDA 510(k)
FDA Class 2
·Microbiology
MODIFICATION TO: LANX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
LANX SPINOUS PROCESS FUSION PLATE
FDA Adverse Event
Injury
·LANX, INC.·Product code KWP·March 17, 2011
ARCHITECT CA 19-9XR
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code NIG·June 24, 2014
2600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 22, 2010
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012