8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Anti Snoring Mouthpiece (L08-BP, L08-PT, L08-BT, L08-TP, L08-TB, L08-PB)
FDA 510(k)
FDA Class 2
·Dental
Ophthalmic Spatulas
FDA UDI
KATENA PRODUCTS, INC.·00841668114322·RUBENSTEIN CORNEAL ROLLER (BX/3)
HeRO Graft
FDA 510(k)
FDA Class 2
·Cardiovascular
Philips IntelliSite Pathology Solution
FDA 510(k)
FDA Class 2
·Pathology
TELIGEN IS-1/DF-1 - DR
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008
EXT DRAINAGE SYSTEM III WITHOUT VENT CATH
FDA Adverse Event
Injury
·CODMAN AND SHURTLEFF - MEDOS·Product code JXG·September 19, 2011
GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 30, 2013
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 16, 2022