# Vortex Surgical, Inc.

- Location (FDA's records): Chesterfield, MO
- FDA decisions: 2 (2019–2022): 2 510(k) clearances
- Product codes: HQB (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 3 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ophthalmed, LLC: 1 (https://510kreport.com/company/ophthalmed)

## Its most-cited devices
- K191846: MAXReach Laser Probe (2019), cited by 1

## Recent decisions
- K220263: Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical Chandeliers (Nov 3, 2022)
- K191846: MAXReach Laser Probe (Dec 23, 2019)

Source page: https://510kreport.com/company/vortex-surgical