27 results · 22ms · 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.

MULTITAK CONICAL TIP BONE SOFT TISSUE SUTURE ANCHOR

FDA 510(k)
FDA Class 2 ·Orthopedic

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033164648·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033164617·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033164624·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033164631·

FOSTER GRANT

FDA UDI
FGX INTERNATIONAL INC.·00193033164600·

ID NOW COVID-19 ASSAY

FDA Adverse Event
Injury ·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·August 3, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Injury ·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·August 3, 2021

ID NOW COVID-19 ASSAY

FDA Adverse Event
Injury ·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·August 3, 2021

ID NOW COVID-19

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·January 5, 2021

PALCERAM 53

FDA 510(k)
FDA Class 2 ·Dental

INSTANT-VIEW MORPHINE (2000) URINE DIP STRIP TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

COMFORT

FDA Adverse Event
Malfunction ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 3, 2025

AVAULTA SOLO ANTERIOR SYNTHETIC SUPPORT SYSTEM

FDA Adverse Event
Injury ·BARD SHANNON LIMITED·Product code FTL·March 14, 2013

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·March 8, 2011

DURATA STS OPTIM PASSIVE FIXATION

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·August 14, 2014

UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011

UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011

UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JJE·December 22, 2011

UNICEL® DXI 600 ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code MMI·December 22, 2011