8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
P/2000
FDA 510(k)
FDA Class 2
·General Hospital
Damon 3MX
FDA UDI
ORMCO CORPORATION·00889989002287·L1 and 2L DAMON3 MX 22 -1/2/0
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690191025·AK3 Flat Insert Trial Size 4-6 - 11mm
INTRASITE GEL (LABELING REVISION)
FDA 510(k)
FDA Class 1
·General Hospital
SCRUB MATE DRY STERILE SCRUB BRUSH
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
INVACARE SOLACE SPS1080 MATTRESS
FDA Adverse Event
FOAM CRAFT A DIV OF FUTURE FOAM INC.·Product code IKY·January 29, 2013
DURASUL COCR HEAD 38/-4 S 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·December 23, 2010
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 18, 2014