# VertigoDx, Inc.

- Location (FDA's records): Wilmington, DE
- FDA decisions: 1 (2026–2026): 1 510(k) clearance
- Product codes: GWN (1)
- Predicates its devices cite: 1 (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

## Firms whose devices it cites most
- Dizzydoctor Systems, LLC: 1 (https://510kreport.com/company/dizzydoctor-systems)

## Recent decisions
- K260566: SMARTVERTIGO™ Vestibular Assessment System (Jul 30, 2026)

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