11 results
·
21ms
·
Sources: EU EUDAMED, US FDA
DTX-200 BONE DENSITOMETER
FDA 510(k)
FDA Class 2
·Radiology
Corin TriFit CF Hip Stem
FDA UDI
CORIN LTD·05055343898475·TriFit™ CF Stem Lateralized Size 11
Barco
FDA UDI
Barco NV·05415334025134·MDRC-2321 SNIB
Sklar
FDA UDI
SKLAR CORPORATION·40649111212131·DISP CHILD RING-TIP EAR CUR 50
COMPETITOR UNICONDYLAR KNEE TIBIAL BASEPLATE
FDA 510(k)
FDA Class 2
·Orthopedic
SURGISEAL Topical Skin Adhesive, SURGISEAL Stylus Topical Skin Adhesive, SURGISEAL Twist Topical Skin Adhesive
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SCREW,FIXATION,BONE
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·May 18, 2015
FOLEY CATHETER, 16FR SILICONE
FDA Adverse Event
Injury
·MEDLINE INDUSTRIES, INC.·Product code NWR·May 23, 2014
ALARIS PUMP MODULE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FPA·January 16, 2013
CRYSTALENS HD
FDA Adverse Event
Injury
·BAUSCH + LOMB·Product code NAA·January 11, 2011
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·July 27, 2015