309 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MAXLOCK EXTREME SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Likorall™ overhead lift
FDA UDI
Liko AB·00887761979710·Overhead track patient lifting/transfer system
RUSCH
FDA UDI
TELEFLEX INCORPORATED·34026704624028·
ArgenZ HT+ 98x12 D3
FDA UDI
ARGEN CORPORATION, THE·D818122005·Dental porcelain/ceramic restoration kit
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690126492·Adjustable Modular Tibia Tray Trial Size 5
SYNTHES MIDFACE DISTRACTOR
FDA 510(k)
FDA Class 2
·Dental
ALLURA XPER OR TABLE SERIES
FDA 510(k)
FDA Class 2
·Radiology
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236592·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236561·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236530·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236585·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236578·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236547·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236554·
PERSONA® Vivacit-E®
FDA UDI
Zimmer, Inc.·00889024236523·
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124015·Tibial cutting block L-5°
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·May 5, 2006
SALUTE FIXATION DEVICE
FDA Adverse Event
Malfunction
·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·April 3, 2006
SYNCHROMED II
FDA Adverse Event
Injury
·NEUROLOGICAL DIV, MEDTRONIC, INC.·Product code LKK·January 27, 2006
MESH-COMPOSIX KUGEL
FDA Adverse Event
Malfunction
·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·December 13, 2005