# NAA: Lens, Intraocular, Accommodative

- Device class: 3; regulation: 21 CFR 886.3600; FDA's rule: PMA required
- FDA decisions: 1
- Recalls: 1 (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)
- 2003: 1
- 2004: 2
- 2005: 3
- 2006: 1
- 2007: 6
- 2008: 4
- 2009: 3
- 2010: 1
- 2011: 4
- 2022: 2

## Most-cited predicates

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