# K214084: hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS

- Pathway: 510(k) (Special)
- Applicant: Cefla S.C.
- Decided: Jan 20, 2022 after 24 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: 1 generation back to K190496 (2019). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K190496: hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS, Cefla S.C. (2019) Summary page 4.

## Most influential descendants
- K223794: hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS (2023), 0 descendants of its own

## Indications for use
hyperion X9 pro, NewTom GiANO HR, X-RADiUS TRiO PLUS is digital panoramic, cephalometric and tomographic extra-oral system, intended to: () produce orthopanoramic images of the maxillofacial region and carry out diagnostic examination on teeth, dental arches and other structures in the oral cavity; (II) produce radiographs of jaws, parts of the skull and carpus for the purpose of cephalometric examination, if equipped with tele-radiographic arm (CEPH); (II1) the production of tomographic images of the head, including the ear, nose and throat (ENT), of the dento-maxillofacial complex, teeth, mandible and maxilla, temporomandibular-articular joint (TMJ), other areas of the human skull and neck with sections of the cervical spine for use in diagnostic support, if equipped with the CBCT option. The device is operated and used by physicians, dentists, x-ray technologists and other legally qualified professionals.

Source page: https://510kreport.com/device/K214084
Methodology: https://510kreport.com/methodology