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FDA 510(k)

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)

K-Number: K260830 · 2026-03-18

Decision Date2026-03-18
Product CodeLBH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) is the device name listed in this FDA 510(k) record. The listed applicant is Sangi Co., Ltd.. It received FDA 510(k) clearance on 2026-03-18 under 510(k) 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. The listed applicant is Sangi Co., Ltd.. The 510(k) number is K260830.

When did APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) receive FDA 510(k) clearance?

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

Who is the listed applicant for APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste)?

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

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

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.

Other records listing Sangi Co., Ltd. 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: LBH)

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.