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FDA 510(k)

Chiavaye Personal Moisturizer

K-Number: K251011 · 2025-12-19

ApplicantUnipack, LLC
Decision Date2025-12-19
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Chiavaye Personal Moisturizer is the device name listed in this FDA 510(k) record. The listed applicant is Unipack, LLC. It received FDA 510(k) clearance on 2025-12-19 under 510(k) number K251011. 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 Chiavaye Personal Moisturizer?

Chiavaye Personal Moisturizer is a medical device that received FDA 510(k) clearance on 2025-12-19. The listed applicant is Unipack, LLC. The 510(k) number is K251011.

When did Chiavaye Personal Moisturizer receive FDA 510(k) clearance?

Chiavaye Personal Moisturizer received FDA 510(k) clearance on 2025-12-19, under 510(k) number K251011.

Who is the listed applicant for Chiavaye Personal Moisturizer?

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

What is the FDA product code for Chiavaye Personal Moisturizer?

The FDA product code for Chiavaye Personal Moisturizer 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.

K261905BUM OilBumlicious, LLC (DBA “Bumlicious”)K261177PINKSLIP Water-Based Personal Lubricant and MoisturizerPINKSLIP, LLCK261909Plum Vagiceuticals™ Vaginal Moisturizing SuppositoriesPCCA, Inc.K254011Flow Water-Based Personal LubricantLBDO Group, Inc.K261292PR Water-Base Lube Personal Lubricant (PR Water-Base Lube Personal Lubricant)PR Personal Care LaboratoriesK252914Sutil Pure Personal Lubricant (models 1148, 1145, 1146, 1147)Hathor Professional Skincare , Ltd.

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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