# Ultimate Wireforms, Inc.

- Location (FDA's records): Terryville, CT
- FDA decisions: 6 (1992–1996): 6 510(k) clearances
- Product codes: DZC (5), EAT (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
- K960799: Ortho-Ice (May 9, 1996)
- K924805: Orthodontic Arch Wire (Mar 31, 1993)
- K923837: Dimpled Multi Modulus Arch Wire (Mar 31, 1993)
- K923836: .016' X .016 Nickel Titanium Uprighting Spring (Dec 23, 1992)
- K923838: The Ultimate RCS Arch Wire (Dec 4, 1992)
- K923839: Nitinol Gentle Touch Coil Spring (Oct 15, 1992)

Source page: https://510kreport.com/company/ultimate-wireforms