# HQG: Lens, Spectacle, Non-Custom (Prescription)

- Device class: 1; regulation: 21 CFR 886.5844; FDA's rule: 510(k) exempt
- FDA decisions: 56
- Recalls: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1982: 3
- 1983: 1
- 1984: 6
- 1985: 7
- 1986: 9
- 1987: 4
- 1988: 6
- 1990: 1
- 1992: 1
- 1994: 1

## Most-cited predicates

Source page: https://510kreport.com/product-code/HQG
Data by year (CSV): https://510kreport.com/product-code/HQG.csv