Archworx— 510(k) K173738
Substantially EquivalentUtah Medical Products and Services
FDA 510(k) clearance K173738 for Archworx, Substantially Equivalent on 2021-02-26. Applicant: Utah Medical Products and Services. Device class: 2.
Clearance details
- Applicant
- Utah Medical Products and Services
- Product code
- Code NXC
- Device class
- Class 2
- Regulation
- 21 CFR 872.5470
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Murray, UT, US
Recent devices under product code NXC
view allAdverse events under product code NXC
product code NXC- Injury
- 15,206
- Malfunction
- 2,576
- Other
- 9
- Total
- 17,791
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.