9 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Artemis Eye System
FDA 510(k)
FDA Class 2
·Neurology
Ophthalmic Retractor
FDA UDI
KATENA PRODUCTS, INC.·00841668101100·HELVESTON "GREAT BIG BARBIE" RETRACTOR 11MM
TVC IMAGING SYSTEM, TVC INSIGHT CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ORIGIN ZIRCONIA
FDA 510(k)
FDA Class 2
·Dental
ENDOWRIST
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC·Product code NAY·October 6, 2022
RSVR MMT-326A 10PK PRDGM 1.8ML 13L
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code FMF·October 6, 2008
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 26, 2013
VAGINAL MESH
FDA Adverse Event
Injury
·UNKNOWN·Product code FTL·July 29, 2011
ESTEEM
FDA Adverse Event
Injury
·ENVOY MEDICAL CORPORATION·Product code OAF·August 29, 2019