47 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Implant, Endosseous, Root-Form
FDA Pre-Market Approval
FDA Class 2
·ALVEOFORM TM BIOGRAFT
Bone Grafting Material, Animal Source
FDA Pre-Market Approval
FDA Class 2
·ALVEOFORM TM BIOGRAFT
Bone Grafting Material, Animal Source
FDA Pre-Market Approval
FDA Class 2
·ALVEOFORM TM BIOGRAFT
Bone Grafting Material, Animal Source
FDA Pre-Market Approval
FDA Class 2
·ALVEOFORM TM BIOGRAFT
Bone Grafting Material, Animal Source
FDA Pre-Market Approval
FDA Class 2
·ALVEOFORM TM BIOGRAFT
Bone Grafting Material, Animal Source
FDA Pre-Market Approval
FDA Class 2
·ALVEOFORM TM BIOGRAFT
Trimline
FDA UDI
ORMCO CORPORATION·00889989051537·UPPER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 12
LEONE SPA
FDA UDI
LEONE SPA·08033707031949·WEB 1ST MOLAR BANDS n.LR 12
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310860012CFG1·NTI Diamond Coarse FG
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837015992·
Electroplated diamond RA 860 012
FDA UDI
Diaswiss SA·07630049951358·Dental diamond instrument for intraoral use
Persona®
FDA UDI
Zimmer, Inc.·00889024552531·
Persona®
FDA UDI
Zimmer, Inc.·00889024552487·
Persona®
FDA UDI
Zimmer, Inc.·00889024552432·
Test, Hepatitis B (B Antigen, B Surface Antigen, Be Antigen)
FDA Pre-Market Approval
FDA Class 2
·AXSYM CORE 2.0 AND AXSYM CORE 2.0 CONTROLS
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·LIFEPAK CR® Plus Defibrillator, LIFEPAK EXPRESS® Defibrillator, and CHARGE-PAK® Battery Charger
APEX MONORAIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·June 19, 2009
APEX MONORAIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·June 8, 2009
MAVERICK2 MONORAIL PTCA CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·April 19, 2007
SHORELINE
FDA Adverse Event
Malfunction
·SEASPINE, INC·Product code OVE·December 16, 2021