# K123823: Interlig

- Pathway: 510(k) (Traditional)
- Applicant: Angelus Industria DE Productos Odontologicos
- Decided: May 31, 2013 after 170 days
- Product code: EBF (Material, Tooth Shade, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K972985 (1997). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972985: Splint IT, Jeneric/Pentron, Inc. (1997) Summary page 1.

## Indications for use
Interlig Is Ind icated for: - Splinting periodontal involved and mobile teeth to prevent movement - To reinforce full denture and partial denture repairs - As a matrix between abutment teeth for receiving a temporary replacement tooth - As an aid In the reinforcement of temporary crowns and bridge work - As a space maintainer for orthodontic Involved teeth

Source page: https://510kreport.com/device/K123823
Methodology: https://510kreport.com/methodology