FDA 510(k)

Clear Miracle

K-Number: K251616 · 2025-07-22

Decision Date2025-07-22

Product CodeNXC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Clear Miracle is the device name listed in this FDA 510(k) record. The listed applicant is Ods Co., Ltd.. It received FDA 510(k) clearance on 2025-07-22 under 510(k) number K251616. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Clear Miracle?

Clear Miracle is a medical device that received FDA 510(k) clearance on 2025-07-22. The listed applicant is Ods Co., Ltd.. The 510(k) number is K251616.

When did Clear Miracle receive FDA 510(k) clearance?

Clear Miracle received FDA 510(k) clearance on 2025-07-22, under 510(k) number K251616.

Who is the listed applicant for Clear Miracle?

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

What is the FDA product code for Clear Miracle?

The FDA product code for Clear Miracle is NXC.

Related Devices (Code: NXC)

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.

K260527FACE4D AlignerAvinent Implant System S.L.U.K260788Smylio AlignersSmylio, Inc.K260722SureSmile Aligner (ASSY500020)Dentsply Sirona, Inc.K253282ZSmile SystemDror Orthodesign , Ltd.K251454Clear Aligner (SCF-3348)Beame Medical Technology (Shenzhen) Limited K250739Primeprint Direct AlignerDreve Dentamid GmbH

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.