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FDA 510(k)

Midas Restore

K-Number: K260661 · 2026-04-15

ApplicantSprintray, Inc.
Decision Date2026-04-15
Product Code
DecisionSubstantially Equivalent

Device Summary

Midas Restore is a medical device manufactured by Sprintray, Inc.. It received FDA 510(k) clearance on 2026-04-15 under approval number K260661. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Midas Restore?

Midas Restore is a medical device that received FDA 510(k) clearance on 2026-04-15. It is manufactured by Sprintray, Inc.. The 510(k) number is K260661.

When was Midas Restore approved by the FDA?

Midas Restore received FDA 510(k) clearance on 2026-04-15, under approval number K260661.

What company makes Midas Restore?

Midas Restore is manufactured by Sprintray, Inc..

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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