8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
CANYONS BI-DIRECTIONAL CHECK VALVE
FDA 510(k)
FDA Class 1
·General Hospital
ANTI-GBM ANTIBODIES QUANTITATIVE KIT
FDA 510(k)
FDA Class 2
·Immunology
IN-VITRO TEST DETERMINATION OF ALBUMIN
FDA 510(k)
FDA Class 2
·Clinical Chemistry
LOGIC PSC TIB INS SZ 4 17MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·February 15, 2024
DEPUY ASR XL FEM IMP SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·February 11, 2013
2124215-2010-24118
FDA Adverse Event
Injury
·GUIDANT PUERTO RICO BV·Product code LWS·January 10, 2011
UNKNOWN DEPUY ASR ACETABULAR CUP
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·July 23, 2014
ev3 Pipeline Flex Embolization Device with Shield Technology. Sold OUS. For neurological endovascular use.
FDA Enforcement
Class I
·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020