# K242185: Rextar Pro

- Pathway: 510(k) (Traditional)
- Applicant: Raypia Co., Ltd.
- Decided: Dec 4, 2024 after 132 days
- Product code: EHD (Unit, X-Ray, Extraoral With Timer)
- Device class: 2
- Regulation: 21 CFR 872.1800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K000061 (2000). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132041: Rextar X, Meta Biomed, Inc. (2013) Summary page 5.

## Indications for use
REXTAR PRO is a portable X-ray system to be used by trained dentists and dental technicians as a mobile, extraoral x-ray source for producing diagnostic x-ray images using intraoral image receptors. It is intended for adult patients.

Source page: https://510kreport.com/device/K242185
Methodology: https://510kreport.com/methodology