# EIX: Probe, Periodontic

- Device class: 1; regulation: 21 CFR 872.4565; 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)
- 1982: 1
- 1987: 2
- 1988: 2
- 1989: 1
- 1994: 2
- 1996: 1

## Most-cited predicates
- K875076: Florida Probe (1988), cited by 2

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