FDA 510(k)

Custom Clear Aligner System

Numéro K : K173785 · 2018-03-13

Date de décision2018-03-13

Code produitNXC

Comité consultatifDE

DécisionSubstantially Equivalent

Résumé du dispositif

Custom Clear Aligner System is the device name listed in this FDA 510(k) record. The listed applicant is Derby Dental Laboratory. It received FDA 510(k) clearance on 2018-03-13 under 510(k) number K173785. 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 Custom Clear Aligner System?

Custom Clear Aligner System is a medical device that received FDA 510(k) clearance on 2018-03-13. The listed applicant is Derby Dental Laboratory. The 510(k) number is K173785.

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

Custom Clear Aligner System received FDA 510(k) clearance on 2018-03-13, under 510(k) number K173785.

Who is the listed applicant for Custom Clear Aligner System?

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

What is the FDA product code for Custom Clear Aligner System?

The FDA product code for Custom Clear 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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