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PMA de la FDA

Lens, contact, orthokeratology, overnight

Número de PMA: P220015 · 2026-08-05

SolicitanteTianjin MasterVision Technology Co., Ltd.
Fecha de decisión2026-08-05
Número PMAP220015
Código de productoNUU
Clase del dispositivoClase 3
Especialidad médicaO
Número de regulación21 CFR 8
Comité asesorOP

Resumen del dispositivo

Lens, contact, orthokeratology, overnight is the device name listed in this FDA 510(k) record. The listed applicant is Tianjin MasterVision Technology Co., Ltd.. It received FDA 510(k) clearance on 2026-08-05. The device is classified under product code NUU. It was reviewed by the OP advisory panel.

Preguntas frecuentes

What is the Lens, contact, orthokeratology, overnight?

Lens, contact, orthokeratology, overnight is a medical device that received FDA 510(k) clearance on 2026-08-05. The listed applicant is Tianjin MasterVision Technology Co., Ltd..

When did Lens, contact, orthokeratology, overnight receive FDA 510(k) clearance?

The clearance date for Lens, contact, orthokeratology, overnight can be found in the official FDA records.

Who is the listed applicant for Lens, contact, orthokeratology, overnight?

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

What is the FDA product code for Lens, contact, orthokeratology, overnight?

The FDA product code for Lens, contact, orthokeratology, overnight is NUU.

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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.

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