# MLP: Keratoprosthesis, Temporary Implant, Surgical Use

- Device class: 2; regulation: 21 CFR 886.3400; FDA's rule: 510(k) required
- FDA decisions: 5
- 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)
- 1984: 1
- 1989: 1
- 1990: 1
- 1991: 1
- 2026: 1

## Most-cited predicates
- K910828: Landers Wide Field Temporary Keratoprosthesis (1991), cited by 1

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