# K131151: Endocenter

- Pathway: 510(k) (Traditional)
- Applicant: Satelec - Acteon Group
- Decided: Jan 16, 2014 after 268 days
- Product code: ELC (Scaler, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 872.4850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K942139 (1995). 9 ancestors in all.
No later device cites it as a predicate yet.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111623: I-Endo Dual, Satelec - Acteon Group (2012) Summary page 3.
- K050895: Surpasson P5 Newtron, Satelec (2005) Summary page 3.

## Indications for use
For use by dentists in standard endodontic procedures using rotary endodontic files or reciprocating endodontic files or use by dentists in periodontics, endodontics, scaling, prosthesis procedures with ultrasonic tips.

Source page: https://510kreport.com/device/K131151
Methodology: https://510kreport.com/methodology