25 results · 50ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Smile Shapers

FDA UDI
Phase Ortho, Inc.·00860006274337·Smile Shapers Retainer

Smile Shapers

FDA UDI
Phase Ortho, Inc.·00860006274320·Smile Shapers Clear Aligner - Zendura

Phase Ortho Private Label

FDA UDI
Phase Ortho, Inc.·00860006274344·Phase Ortho Private Label Clear Aligner - Tempo...

Tru-Smile

FDA UDI
Phase Ortho, Inc.·00860006274375·Tru-Smile Retainers

Tru-Smile

FDA UDI
Phase Ortho, Inc.·00860006274368·Tru-Smile Clear Aligner

Phase Ortho

FDA UDI
Phase Ortho, Inc.·00860006274306·Phase Ortho Clear Aligner

Phase Ortho Private Label

FDA UDI
Phase Ortho, Inc.·00860006274351·Phase Ortho Private Label Retainer - Temporary ...

Phase Ortho

FDA UDI
Phase Ortho, Inc.·00860006274313·Phase Ortho Retainer

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

ANTI-D BIOCLONE

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·August 10, 2009

ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

FDA Adverse Event
Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009