# Aneuvo

- Location (FDA's records): Los Angeles, CA
- FDA decisions: 1 (2026–2026): 1 510(k) clearance
- Product codes: SDO (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
- Onward Medical, Inc.: 1 (https://510kreport.com/company/onward-medical)

## Recent decisions
- K252893: ExaStim® Stimulation System (EXA-001); ExaStim® Stimulation System (EXA-011); ReCure® Electrode Pad (PAD-003); ReCure® Electrode Pad (PAD-013) (Mar 27, 2026)

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