# K020206: Intraoral Camera ME-15

- Pathway: 510(k) (Traditional)
- Applicant: Dent Corp. Research & Development
- Decided: Apr 11, 2002 after 79 days
- Product code: EIA (Unit, Operative Dental)
- Device class: 1
- Regulation: 21 CFR 872.6640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Indications for use
The ME-15 Intraoral Camera use only for photegraphing from a full mouth to a signal tooth. The ME-15 is not intended for any other use.

Source page: https://510kreport.com/device/K020206
Methodology: https://510kreport.com/methodology