# K253009: DS Core Detect

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply Sirona, Inc.
- Decided: Jan 7, 2026 after 110 days
- Product code: MYN (Analyzer, Medical Image)
- Device class: 2
- Regulation: 21 CFR 892.2070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to P980025 (1998). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232384: Videa Dental Assist, Videahealth, Inc. (2023) Summary page 5.

## Indications for use
DS Core Detect is a concurrent read, computer assisted detection software intended to aid the dentist in the incidental detection of permanent teeth that may be associated with periapical radiolucencies in CBCT images. The device is not intended as a replacement for a complete dentist's review or a replacement of their clinical judgment. The device is to be used by licensed dentists. The device is designed for patients who already have CBCT data obtained for other reasons. DS Core Detect does not generate X-ray images and does not provide an indication for taking such images. The device is intended for adults aged 22 years and older with permanent teeth.

Source page: https://510kreport.com/device/K253009
Methodology: https://510kreport.com/methodology