With roots in its first medical-device facility opened in 1968, Viant has spent more than five decades building an engineering-led manufacturing business focused entirely on medical technology. The company now helps device OEMs move from development into production through a vertically integrated global network, with particular recognition for its Fremont micro-molding operation, where specialists make highly complex components smaller than a resin pellet.
ISO 13485
ISO 14971
Medical Device Single Audit Program (MDSAP)
FDA Registered
Registration
FDA Quality System Regulation cGMP
Compliance program
ISO Class 7 Cleanroom
ISO Class 8 Cleanroom
FDAREGISTRATION
Quality certification
FDACGMP
Quality certification