Vesalio, Inc.
FDA Regulatory Profile
Vesalio, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 6, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K251097 | V-DAC Catheter | January 6, 2026 |
| K253407 | NeVa PV Thrombectomy Device | November 24, 2025 |
| K251006 | NeVasc Aspiration System | November 10, 2025 |
| K251312 | Vesalio Peripheral System | October 24, 2025 |
| K201085 | NeVa PV Thrombectomy Device | January 15, 2021 |