# K132041: Rextar X

- Pathway: 510(k) (Special)
- Applicant: Meta Biomed, Inc.
- Decided: Jul 31, 2013 after 29 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: 6 generations back to K000061 (2000). 6 ancestors in all.
7 later devices descend from it; 6 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)
- K122016: Rextar, Rextar LCD, Meta Biomed, Inc. (2013) Summary page 2.

## Most influential descendants
- K172810: Port-X IV (2018), 1 descendant of its own
- K242185: Rextar Pro (2024), 0 descendants of its own
- K221587: DHX-70H, XTG-70H (2023), 0 descendants of its own
- K223010: Portable X-ray System (2023), 0 descendants of its own
- K220579: Hybrid C70 (2022), 0 descendants of its own

## Indications for use
REXTAR X is 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 both adult and pediatric subjects.

Source page: https://510kreport.com/device/K132041
Methodology: https://510kreport.com/methodology