23 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HANDPIECE SHEATH-MODEL #A910
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120119291·Steel, round, finishing bur
CoreLink Bifurcated Illuminator
FDA UDI
Lumitex, Inc.·00812432021580·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450224427·
COLOR SPEX
FDA UDI
FGX INTERNATIONAL INC.·00193033346273·
COLOR SPEX
FDA UDI
FGX INTERNATIONAL INC.·00193033338889·
COLOR SPEX
FDA UDI
FGX INTERNATIONAL INC.·00193033338865·
COLOR SPEX
FDA UDI
FGX INTERNATIONAL INC.·00193033338872·
MODIFICATION TO TSRH SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
WAKO AUTOKIT LP(A) AND LP(A) CALIBRATOR/COBAS FARA
FDA 510(k)
FDA Class 2
·Immunology
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code LIT·December 1, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·March 27, 2007
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code DQY·December 28, 2006
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code DQY·March 5, 2007
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 28, 2006
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·January 27, 2012
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code MNI·April 16, 2013
ULTRA-THIN SDS BALLOON CATHETER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORP.·Product code DQY·April 12, 2007
2.0MM IMF SCREW SELF-DRILLING 12MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZL·March 19, 2013
VISIAN ICL (IMPLANTABLE COLLAMER LENS)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code HQL·March 9, 2011