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FDA 510(k)

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)

K-Number: K260830 · 2026-03-18

ApplicantSangi Co., Ltd.
Decision Date2026-03-18
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) is a medical device manufactured by Sangi Co., Ltd.. It received FDA 510(k) clearance on 2026-03-18 under approval number K260830. The device is classified under product code LBH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)?

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) is a medical device that received FDA 510(k) clearance on 2026-03-18. It is manufactured by Sangi Co., Ltd.. The 510(k) number is K260830.

When was APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) approved by the FDA?

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) received FDA 510(k) clearance on 2026-03-18, under approval number K260830.

What company makes APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)?

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) is manufactured by Sangi Co., Ltd..

What is the FDA product code for APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)?

The FDA product code for APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) is LBH.

Related Clinical Trials

NCT07069127 Hydroxyapatite-Based Home Treatment for Dentin Sensitivity in Celiac Patients RECRUITING

Other Devices by Sangi Co., Ltd.

K220419Apapro Desensitizer

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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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