Nexus CMF, LLC
FDA Regulatory Profile
Nexus CMF, LLC has 0 FDA recalls, 4 inspections, 1 510(k) clearance and 0 compliance actions on record.
- Latest inspection
- Sep 25, 2019 · VAI
- Latest 510(k)
- Oct 9, 2026
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Summary
Record counts and when each FDA source was last refreshed
| Records | Count | Last refreshed | Source as of | Status |
|---|
| Recalls | 0 | Nov 4, 2026 (checked Nov 8, 2026, unchanged) | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 1 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 4 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent FDA Inspections
NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.
FDA-Inspected Facilities
| Facility | Location | Inspections | Latest |
|---|
| FEI 3009702671 | Cottonwood Heights, UT | 4 | Sep 25, 2019 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K260156 | TruVision Single-Use 1.9mm Arthroscopy System | Oct 9, 2026 |