# KAI: Mirror, Ent

- Device class: 1; regulation: 21 CFR 874.4420; FDA's rule: 510(k) exempt
- FDA decisions: 9
- Recalls: 0 (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)
- 1977: 2
- 1979: 1
- 1982: 4
- 1983: 1
- 1984: 1

## Most-cited predicates

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