11 results
·
20ms
·
Sources: EU EUDAMED, US FDA
MICROPOWER HAND PIECE: ORAL MAX HIGH SPEED DRILL
FDA 510(k)
FDA Class 2
·Dental
REMEL
FDA UDI
REMEL, INC.·00848838005961·BHI Broth (5ml) 100/PK
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00681490882767·INSTRUMENT 9060270 LAM SPREADER MOD H
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K0602000·Tray base, 2"
CYLOS DR-T
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO·Product code DTB·November 29, 2006
SETROX S 45
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO·Product code DTB·November 29, 2006
ELECSYS CORTISOL TEST SYSTEM
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TREMOROMETER
FDA 510(k)
FDA Class 2
·Neurology
NEXGEN LPS-FLEX FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code NJL·April 11, 2013
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·April 15, 2011
BOOMERANG CATALYST II SYSTEM
FDA Adverse Event
Injury
·CARDIVA MEDICAL, INC.·Product code DXC·June 10, 2008