7 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
CATS Tonometer Prism
FDA 510(k)
FDA Class 2
·Ophthalmic
PROTHELIAL
FDA 510(k)
FDA Unclassified
·Unknown
CD HORIZON SPINAL SYSTEM GROWTH ROD SET
FDA 510(k)
FDA Class 2
·Orthopedic
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 24, 2011
TOTAL ASR ACET IMP SIZE 56
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·June 17, 2013
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·October 15, 2014
NSK
FDA Adverse Event
Injury
·NAKANISHI INC.·Product code KMW·May 19, 2024