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