# ELR: Post, Root Canal

- Device class: 1; regulation: 21 CFR 872.3810; FDA's rule: 510(k) exempt
- FDA decisions: 35
- 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)
- 1994: 6
- 1995: 2
- 1997: 1
- 1998: 3
- 2000: 4
- 2001: 1
- 2002: 4
- 2003: 1
- 2004: 1
- 2006: 1

## Most-cited predicates
- K983266: Fibrekor Post System (1998), cited by 2
- K945370: C-POST (1995), cited by 2
- K000311: Parapost Fiber White (2000), cited by 2
- K003221: Harald Nordin Glassix Glass Fiber Composite Dental Post (2000), cited by 2
- K012354: Snowpost, Snowlight (2001), cited by 2
- K020431: Fibiocore (2002), cited by 1
- K030820: Everstick Post (2003), cited by 1

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