FDA 510(k)

Clear Aligner

N.º K: K213026 · 2022-08-16

SolicitanteShenzhen Meiming Dentistry Technology Co., Ltd.

Fecha de decisión2022-08-16

Código de productoNXC

Comité asesorDE

DecisiónSubstantially Equivalent

Resumen del dispositivo

Clear Aligner is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Meiming Dentistry Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-08-16 under 510(k) number K213026. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Clear Aligner?

Clear Aligner is a medical device that received FDA 510(k) clearance on 2022-08-16. The listed applicant is Shenzhen Meiming Dentistry Technology Co., Ltd.. The 510(k) number is K213026.

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

Clear Aligner received FDA 510(k) clearance on 2022-08-16, under 510(k) number K213026.

Who is the listed applicant for Clear Aligner?

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

What is the FDA product code for Clear Aligner?

The FDA product code for Clear Aligner is NXC.

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Dispositivos relacionados (Código: NXC)

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Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.