# K992233: Apex Locator Bingo-1020

- Pathway: 510(k) (Traditional)
- Applicant: Dent Corp. Research & Development
- Decided: Nov 30, 1999 after 158 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
No predicates in its family tree.
13 later devices descend from it; 2 cite it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K111474: Bingo Pro (2011), 11 descendants of its own
- K131907: Raypex 6 (2014), 9 descendants of its own
- K191806: Propex IQ Apex Locator (2019), 5 descendants of its own
- K203836: BOMEDENT Apex locator, WISMY Apex locator (2021), 4 descendants of its own
- K181087: Apex Locator, DPEX III (2018), 2 descendants of its own

## Indications for use
BINGO-1020 is a modern device for precise apex localization during root channel treatment. BINGO-1020 is distinguished by increasing precision at 0.1mm on wet/dry, large graphic display where current position of endo file is reflected and other essential information is displayed.

Source page: https://510kreport.com/device/K992233
Methodology: https://510kreport.com/methodology