Data / Medical devices / United States / Utah Medical Products And Services
Utah Medical Products And Services: FDA-registered device maker in Murray, UT, United States, 2 510(k) clearances
Utah Medical Products And Services is registered with the FDA (registration 3010881820) in Murray, UT, United States. It lists 3 device types. The FDA files 2 510(k) clearances under its listings, the newest dated February 26, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010881820
- Address
- 6526 South State St Suite #301, Murray, UT, United States, 84107
- Owner or operator
- Utah Medical Products and Services (10084309)
- Roles
- Contract manufacturer, Manufacturer, Repackager or relabeler
- First device listed
- February 8, 2022
- Registered through
- 2026
- Brand names listed
- Archworx, BIO-RAY A-1 Anchor Screw System, Vivos Pex
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Aligner, Sequential | NXC | 2 | Manufacturer | accessdata.fda.gov |
| Clamp, Wire, Orthodontic | ECN | 1 | Contract manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Orthodontic | OAT | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 26, 2021 | K173738 | Archworx | NXC | Substantially Equivalent | Utah Medical Products and Services | accessdata.fda.gov |
| November 6, 2019 | K182929 | BIO-RAY A-1 Anchor Screw System | OAT | Substantially Equivalent | Microware Precision Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Aligner, Sequential
- All makers of Clamp, Wire, Orthodontic
- All makers of Implant, Endosseous, Orthodontic
Updated February 26, 2021. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.