# Vxtra Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 10 (1980–1983): 10 510(k) clearances
- Product codes: HQC (3), GES (2), HNN (2), GEI (1), DRX (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K832938: Ocutome Paratubing Set (Oct 19, 1983)
- K832980: Vxtra Ocutome Kit (Oct 19, 1983)
- K831266: Microsurgical Knife (Jun 10, 1983)
- K830385: Irrigation/Aspiration Kit (Apr 5, 1983)
- K830379: Phako Kit (Apr 5, 1983)
- K812620: Adjustable Microsurgical Knife (Oct 19, 1981)
- K812526: Micro Blade II (Sep 16, 1981)
- K812160: Microsurgical Blade (Aug 31, 1981)

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