7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
BOUNDARY TUBING HOLDERS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
SIDEPORT PINCH CLAMP DEVICE
FDA 510(k)
FDA Class 2
·General Hospital
ABSOLUTE WHITE LIGHT
FDA 510(k)
FDA Class 1
·Dental
GLIDESCOPE GVL 5
FDA Adverse Event
Malfunction
·VERATHON MEDICAL ULC.·Product code CCW·March 19, 2014
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 2, 2007
SPRINT QUATTRO
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·October 31, 2012
Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm; intended for use in long bone fractures, the fixation of osteopenic bone, the fixation of osteotomies, and for the fixation of non-unions and malunions.
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·September 30, 2015