# K260661: Midas Restore

- Pathway: 510(k) (Traditional)
- Applicant: Sprintray, Inc.
- Decided: Apr 15, 2026 after 44 days
- 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 K042819 (2004). 31 ancestors in all.
No later device cites it as a predicate yet.
0 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K222623: Digital Crown, Sprintray, Inc. (2022) Summary page 5.

## Indications for use
Midas Restore is a light-curable polymerizable resin intended to be used for the fabrication of individual and fixed definitive full single crowns; definitive partial crowns (e.g., inlays, onlays) in anterior and posterior area, individual and fixed single veneers; artificial teeth for dental prostheses, which are used for removable definitive full dentures in dental offices and laboratories. The material is an alternative to traditional restorative dental material.

Source page: https://510kreport.com/device/K260661
Methodology: https://510kreport.com/methodology