Manufacturer registered with FDA
Utah Medical Products and Services
Murray, UT, United States. Lists 3 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 3
- Brands and models
- 3
- 510(k) clearances
- 12021–2021
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 2007–2026
Devices listed with FDA
What Utah Medical Products and Services currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Orthodontic Wire ClampECN · Class 1 | — | Maker | Vivos Pex | 2022 |
| Sequential AlignerNXC · Class 2 | Clear aligners | Maker | Archworx | 2022 |
| Orthodontic Endosseous ImplantOAT · Class 2 | — | Lister | BIO-RAY A-1 Anchor Screw System | 2024 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Utah Medical Products and Services lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Microware Precision Co., Ltd. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 6 Nov 2019 | K182929 | BIO-RAY A-1 Anchor Screw System | Microware Precision Co., Ltd. | OAT Orthodontic Endosseous Implant |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| UTAH MEDICAL PRODUCTS AND SERVICESFDA reg. 3010881820 | Murray, UT, United States | Contract manufacturer, Manufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10084309). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.