1,989 results · 33ms · Sources: EU EUDAMED, US FDA

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Orthonol

FDA UDI
Rmo, Inc.·00885797016195·D425174

Amplion Care Assurance

FDA UDI
AMPLION CLINICAL COMMUNICATIONS, INC.·00850016398314·Zone Controller (ZC), Version 1.2

WIRE 24GA PRESTRETCH 10/PK 6IN

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code DZL·November 15, 2016

3M UNITEK NITINOL CL OFIII OVOID L014

FDA Adverse Event
Malfunction ·3M UNITEK CORPORAION·Product code DZC·December 19, 2016

CUNITI WIRE

FDA Adverse Event
Injury ·ORMCO CORPORATION·Product code DZC·December 2, 2016

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORPORATION·Product code DZC·February 3, 2009

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORPORATION·Product code DZC·March 9, 2009

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORPORATION·Product code DZC·January 6, 2010

PERMACHROME STANDARD STAINLESS STEEL STRIAGHT ARCH WIRE

FDA Adverse Event
Injury ·3M UNITEK·Product code DZC·February 16, 2004

INBRACE

FDA Adverse Event
Injury ·SWIFT HEALTH SYSTEMS, INC·Product code DZC·May 27, 2021

INBRACE

FDA Adverse Event
Injury ·SWIFT HEALTH SYSTEMS, INC·Product code DZC·May 25, 2021

INBRACE

FDA Adverse Event
Injury ·SWIFT HEALTH SYSTEMS, INC·Product code DZC·May 26, 2021

BRIUS

FDA Adverse Event
Injury ·BRIUS·Product code DZC·May 3, 2022

BETA TITANIUM ARCH

FDA Adverse Event
Malfunction ·ACME MONACO·Product code DZC·August 22, 2000

HI-T II ARCHWIRE

FDA Adverse Event
Injury ·3M UNITEK·Product code DZC·August 31, 2000

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORP.·Product code DZC·April 16, 2007

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORP.·Product code DZC·April 16, 2007

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORP.·Product code DZC·April 16, 2007

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORP.·Product code DZC·May 17, 2007

DAMON COPPER NITI WIRE

FDA Adverse Event
Malfunction ·ORMCO CORP.·Product code DZC·May 17, 2007