Company ยท US
Vein 360, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2019 to 2026. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (1 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 |
|---|---|---|---|
| Oct 20, 2026 | K260708 | Vein360 Reprocessed LithoVue Digital Flexible Ureteroscope (Standard Deflection); Vein360 Reprocessed LithoVue Digital F Vein 360 | FGB |
| Oct 24, 2023 | K232584 | Vein360 Reprocessed Visions PV.014P Rx Digital IVUS Catheter, Vein360 Reprocessed Eagle Eye Platinum Rx Digital IVUS Cat Vein 360, LLC | OWQ |
| Aug 25, 2023 | K230928 | Vein360 Reprocessed Visions PV.018 Digital IVUS Catheter Vein 360, LLC | OWQ |
| Jun 6, 2023 | K230584 | Vein360 Reprocessed Visions PV.035 Digital IVUS Catheter Vein 360, LLC | OWQ |
| Oct 22, 2019 | K191073 | Vein360 Endovenous Radiofrequency Ablation (RFA) Catheter Vein 360, LLC | NUJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||