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FDA 510(k)

ThinkQA 3

K-Number: K252937 · 2026-06-12

ApplicantDosisoft SA
Decision Date2026-06-12
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ThinkQA 3 is the device name listed in this FDA 510(k) record. The listed applicant is Dosisoft SA. It received FDA 510(k) clearance on 2026-06-12 under 510(k) number K252937. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ThinkQA 3?

ThinkQA 3 is a medical device that received FDA 510(k) clearance on 2026-06-12. The listed applicant is Dosisoft SA. The 510(k) number is K252937.

When did ThinkQA 3 receive FDA 510(k) clearance?

ThinkQA 3 received FDA 510(k) clearance on 2026-06-12, under 510(k) number K252937.

Who is the listed applicant for ThinkQA 3?

The FDA 510(k) record lists Dosisoft SA as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ThinkQA 3?

The FDA product code for ThinkQA 3 is IYE.

Other records listing Dosisoft SA as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: IYE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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