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Sign in to claim this brandVivorte, Inc
US
Last updated May 31, 2026
Information
- Country
- US
- Address
- —
- Website
- vivorte.com
- —
- —
- [email protected]
- Phone
- 502-714-7234
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 078400984
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Trabexus ® | 5 cc | FDA UDI | Class II | Unknown |
| Wizard CaP | 10 cc | FDA UDI | Class II | Unknown |
| Wizard CaP | 3 cc | FDA UDI | Class II | Unknown |
| Fortera | 5 cc | FDA UDI | Class II | Active |
| Trabexus® | 10 cc | FDA UDI | Class II | Active |
| Trabexus ® | 3 cc | FDA UDI | Class II | Unknown |
| Trabexus ® | 10 cc | FDA UDI | Class II | Unknown |
| Trabexus® | 3 cc | FDA UDI | Class II | Active |
| Fortera | 10 cc | FDA UDI | Class II | Active |
| Trabexus® | 5 cc | FDA UDI | Class II | Active |
| Wizard CaP | 5 cc | FDA UDI | Class II | Unknown |
| Fortera | 3 cc | FDA UDI | Class II | Active |
| Vivorte Bvf | K130703 | FDA 510(k) | Class II | Active |
| Vivorte Bvf Lite | K131133 | FDA 510(k) | Class II | Active |
| Vivorte Trabexus EB | K143547 | FDA 510(k) | Class II | Active |
| Vivorte Trabexus | K143549 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Sep 9, 2018 | Z-2024-2021 | — | terminated | incorrect expiration date- product is listed with 02-15-2019 the correct kit expiration date is 12-18-2018 |