# Vivorte, Inc.

- Location (FDA's records): Fort Wayne, IN
- FDA decisions: 4 (2013–2015): 4 510(k) clearances
- Product codes: MBP (2), MQV (2)
- Predicates its devices cite: 5 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Etex Corp.: 1 (https://510kreport.com/company/etex)

## Its most-cited devices
- K130703: Vivorte BVF (2013), cited by 1
- K131133: Vivorte BVF Lite (2013), cited by 1

## Recent decisions
- K143547: Vivorte Trabexus EB (Jan 14, 2015)
- K143549: Vivorte Trabexus (Jan 14, 2015)
- K130703: Vivorte BVF (Sep 12, 2013)
- K131133: Vivorte BVF Lite (Aug 12, 2013)

Source page: https://510kreport.com/company/vivorte