Founded in 1968, Viant designs and manufactures medical devices and components, offering OEMs an end-to-end partner from engineering and development through production and assembly. Its vertically integrated global network is especially distinctive for combining long-standing precision metal and orthopedic expertise with newer capabilities such as Fremont’s micro-molding operation, where parts smaller than a resin pellet are made in an ISO Class 8 cleanroom. Viant supports medical technology programs with a single-source model that can scale from prototype work to commercial production.
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
FDA
Quality certification
FDACGMP
Quality certification