Resonance Technology, Inc.
FDA Regulatory Profile
Resonance Technology, Inc. has 0 FDA recalls, 5 inspections, 1 510(k) clearance and 0 compliance actions on record.
- Latest inspection
- Oct 17, 2025 · VAI
- Latest 510(k)
- Mar 22, 2000
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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 | 5 | Nov 8, 2026 | Newest record Oct 28, 2026 | Current |
|---|
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
|---|
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|
| Oct 17, 2025 | Northridge, CA | Devices | Voluntary Action Indicated (VAI) | 1000306474 |
| Oct 6, 2022 | Northridge, CA | Devices | No Action Indicated (NAI) | 1000306474 |
| Jul 17, 2019 | Northridge, CA | Devices | No Action Indicated (NAI) | 1000306474 |
| Feb 20, 2015 | Northridge, CA | Devices | Voluntary Action Indicated (VAI) | 1000306474 |
| Nov 9, 2011 | Northridge, CA | Devices | No Action Indicated (NAI) | 1000306474 |
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 1000306474 | Northridge, CA | 5 | Oct 17, 2025 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K994351 | M.R. VISION 2000 ULTRA AUDIO VISUAL SYSTEM / COMMANDER X6 SYSTEM | Mar 22, 2000 |