# K230505: Orthopantomograph™ OP 3D LX

- Pathway: 510(k) (Traditional)
- Applicant: Palodex Group OY
- Decided: Jun 9, 2023 after 105 days
- Product code: OAS (X-Ray, Tomography, Computed, Dental)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K973598 (1997). 20 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K180947: Orthopantomograph OP 3D, Palodex Group OY (2018) Summary page 4.
- K163423: Orthopantomograph OP300, Palodex Group OY (2017) Summary page 4.

## Most influential descendants
- K241249: Orthopantomograph™ OP 3D LX (PAN 3D); Orthopantomograph™ OP 3D LX (PAN CEPH 3D) (2024), 0 descendants of its own

## Indications for use
ORTHOPANTOMOGRAPH™ OP 3D LX is an X-ray device that is intended to be used for imaging of adult and pediatric patients. The device can be configured to take panoramic, cephalometric or 3D images of cranio-maxillofacial complex including the ear, nose and throat (ENT) and airway regions, and cervical spine. The device can be configured to take carpus images. The device is operated and used by qualified healthcare professionals.

Source page: https://510kreport.com/device/K230505
Methodology: https://510kreport.com/methodology