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FDA 510(k)

Morph

K-Number: K260032 · 2026-05-13

ApplicantBeauBrain Healthcare, Inc.
Decision Date2026-05-13
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Morph is a medical device manufactured by BeauBrain Healthcare, Inc.. It received FDA 510(k) clearance on 2026-05-13 under approval number K260032. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Morph?

Morph is a medical device that received FDA 510(k) clearance on 2026-05-13. It is manufactured by BeauBrain Healthcare, Inc.. The 510(k) number is K260032.

When was Morph approved by the FDA?

Morph received FDA 510(k) clearance on 2026-05-13, under approval number K260032.

What company makes Morph?

Morph is manufactured by BeauBrain Healthcare, Inc..

What is the FDA product code for Morph?

The FDA product code for Morph is QIH.

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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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