FDA 510(k)

MyClearALIGN Dental Aligner System

Numéro K : K221475 · 2022-08-31

Date de décision2022-08-31

Code produitNXC

Comité consultatifDE

DécisionSubstantially Equivalent

Résumé du dispositif

MyClearALIGN Dental Aligner System is the device name listed in this FDA 510(k) record. The listed applicant is Key Dental Technologies, LLC. It received FDA 510(k) clearance on 2022-08-31 under 510(k) number K221475. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the MyClearALIGN Dental Aligner System?

MyClearALIGN Dental Aligner System is a medical device that received FDA 510(k) clearance on 2022-08-31. The listed applicant is Key Dental Technologies, LLC. The 510(k) number is K221475.

When did MyClearALIGN Dental Aligner System receive FDA 510(k) clearance?

MyClearALIGN Dental Aligner System received FDA 510(k) clearance on 2022-08-31, under 510(k) number K221475.

Who is the listed applicant for MyClearALIGN Dental Aligner System?

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

What is the FDA product code for MyClearALIGN Dental Aligner System?

The FDA product code for MyClearALIGN Dental Aligner System is NXC.

Essais cliniques associés

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Dispositifs connexes (Code : NXC)

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

Source officielle

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