# K121206: Detect

- Pathway: 510(k) (Traditional)
- Applicant: Forum Engineering Technologies, Ltd.
- Decided: Jan 10, 2013 after 265 days
- Product code: LQY (Locator, Root Apex)
- Device class: U
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K992233 (1999). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111474: Bingo Pro, Forum Engineering Technologies (96), Ltd. (2011)

## Indications for use
Detect is an electronic device used to indicate the location of the apex and the working length. This product must only be used in hospital environents, clinics or dental offices, by qualified practitioners.

Source page: https://510kreport.com/device/K121206
Methodology: https://510kreport.com/methodology