FDA 510(k)

Ohlendorf Clear Aligner

K-Number: K210540 · 2021-05-19

Decision Date2021-05-19

Product CodeNXC

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Ohlendorf Clear Aligner is the device name listed in this FDA 510(k) record. The listed applicant is Ohlendorf Appliance Laboratory. It received FDA 510(k) clearance on 2021-05-19 under 510(k) number K210540. 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 Ohlendorf Clear Aligner?

Ohlendorf Clear Aligner is a medical device that received FDA 510(k) clearance on 2021-05-19. The listed applicant is Ohlendorf Appliance Laboratory. The 510(k) number is K210540.

When did Ohlendorf Clear Aligner receive FDA 510(k) clearance?

Ohlendorf Clear Aligner received FDA 510(k) clearance on 2021-05-19, under 510(k) number K210540.

Who is the listed applicant for Ohlendorf Clear Aligner?

The FDA 510(k) record lists Ohlendorf Appliance Laboratory as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ohlendorf Clear Aligner?

The FDA product code for Ohlendorf Clear Aligner 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.