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FDA 510(k)

Flow Water-Based Personal Lubricant

K-Number: K254011 · 2026-06-22

Decision Date2026-06-22
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Flow Water-Based Personal Lubricant is the device name listed in this FDA 510(k) record. The listed applicant is LBDO Group, Inc.. It received FDA 510(k) clearance on 2026-06-22 under 510(k) number K254011. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Flow Water-Based Personal Lubricant?

Flow Water-Based Personal Lubricant is a medical device that received FDA 510(k) clearance on 2026-06-22. The listed applicant is LBDO Group, Inc.. The 510(k) number is K254011.

When did Flow Water-Based Personal Lubricant receive FDA 510(k) clearance?

Flow Water-Based Personal Lubricant received FDA 510(k) clearance on 2026-06-22, under 510(k) number K254011.

Who is the listed applicant for Flow Water-Based Personal Lubricant?

The FDA 510(k) record lists LBDO Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Flow Water-Based Personal Lubricant?

The FDA product code for Flow Water-Based Personal Lubricant is NUC.

Related Devices (Code: NUC)

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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