Innova Vascular, Inc.
Innova Vascular, Inc. has 0 FDA recalls, 1 inspection, 1 510(k) clearance and 0 compliance actions on record.
- Latest inspection
- Jan 12, 2026 · VAI
- Latest 510(k)
- Jun 1, 2023
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Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Oct 23, 2026 | Not stated | Current |
| 510(k) clearances | 1 | Oct 4, 2026 | Not stated | Current |
| Inspections | 1 | Oct 26, 2026 | Not stated | Current |
| Compliance actions | 0 | Oct 23, 2026 | Not stated | Current |
Recent FDA Inspections
| Date | Site | Product | Classification | FEI |
|---|---|---|---|---|
| Jan 12, 2026 | Irvine, CA | Devices | Voluntary Action Indicated (VAI) | 3020256033 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K223929 | Laguna Clot Retriever System and Malibu Aspiration Catheter System (Laguna Thrombectomy System) | Jun 1, 2023 |