47 results · 26ms · Sources: EU EUDAMED, US FDA

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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