Tendonova Corporation
FDA Regulatory Profile
Tendonova Corporation has 0 FDA recalls, 1 inspection, 1 510(k) clearance and 0 compliance actions on record.
- Latest inspection
- May 16, 2025 · NAI
- Latest 510(k)
- Mar 8, 2022
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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 8, 2026 | File dated Nov 3, 2026 | Current |
|---|
| 510(k) clearances | 1 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
|---|
| Inspections | 1 | Nov 11, 2026 | Newest record Nov 5, 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 3025663926 | Atlanta, GA | 1 | May 16, 2025 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K212049 | Oclet TDS 1000 | Mar 8, 2022 |