Utah Medical Products and Services
United Statesfrom the FDA registration address FDA FEI 3010881820
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Utah Medical Products and Services makes
Utah Medical Products and Services manufactures the Archworx, a spinal fixation system designed for internal orthopedic stabilization, including screws and rods used in surgical procedures for spinal alignment and support.
The company’s portfolio is regulated under FDA’s Class II device classification, with products listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Archworx Ref K173738
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3010881820
- Address
- 6526 South State St, Murray, UT, 84107
Frequently asked questions
How many devices does Utah Medical Products and Services have in the registry?
The registry currently lists 1 device for Utah Medical Products and Services. Devices recorded under merged duplicate company entries are counted once.
Which registries list Utah Medical Products and Services's devices?
Among its 1 most recently registered device, Utah Medical Products and Services has devices listed in FDA 510(k) (1 device).
What risk classes do Utah Medical Products and Services's devices fall under?
Among its 1 most recently registered device, the classes recorded for Utah Medical Products and Services's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Utah Medical Products and Services in the registry?
The most recently registered devices listed for Utah Medical Products and Services include Archworx.