Company ยท US
Vesalio, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2021 to 2026. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (4 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 5, 2026 | K254211 | pVasc Net Mechanical Thrombectomy Device Vesalio, Inc. | |
| Jan 6, 2026 | K251097 | V-DAC Catheter Vesalio, Inc. | QJP |
| Nov 24, 2025 | K253407 | NeVa PV Thrombectomy Device Vesalio, Inc. | QEX |
| Nov 10, 2025 | K251006 | NeVasc Aspiration System Vesalio, Inc. | NRY |
| Oct 24, 2025 | K251312 | Vesalio Peripheral System Vesalio, Inc. | QEZ |
| Jan 15, 2021 | K201085 | NeVa PV Thrombectomy Device Vesalio | QEW |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||