# Ultroid, LLC

- Location (FDA's records): Carson City, NV
- FDA decisions: 2 (2003–2003): 2 510(k) clearances
- Product codes: KNS (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K030315: Modification to Ultroid Hemorrhoid Management System (Feb 27, 2003)
- K023706: Ultroid Hemorrhoid Management System (Jan 14, 2003)

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