8 results
·
37ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KINEMATIC III POST CRUCIATE TOTAL CONDYLAR KNEE SY
FDA 510(k)
FDA Class 2
·Orthopedic
Ecosite Bulk Fill
FDA 510(k)
FDA Class 2
·Dental
DINAMAP MODEL 825A
FDA 510(k)
FDA Class 2
·Cardiovascular
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·August 6, 2020
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 13, 2014
INTEGRATED APD SET W/CASSETTE3 PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 15, 2010
CORAIL2 NON COL HO SIZE 9
FDA Adverse Event
Injury
·DEPUY FRANCE SAS - 3003895575·Product code KWA·December 13, 2012
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 3, 2017