# Frontier Products

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1980–1983): 4 510(k) clearances
- Product codes: DXQ (2), DXP (1), HTH (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
- K831001: Unicuff-Blood Pressure Cuff (Jul 28, 1983)
- K822305: Ortho-Level (Aug 20, 1982)
- K812639: Unicuff (Oct 2, 1981)
- K801099: Unicuf, Blood Pressure Cuff (May 30, 1980)

Source page: https://510kreport.com/company/frontier-products