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FDA 510(k)

Zfx Abutments

N.º K: K231915 · 2024-03-01

SolicitanteZfx GmbH - A Company of Zimvie
Fecha de decisión2024-03-01
Código de productoNHA
Comité asesorDE
DecisiónSubstantially Equivalent

Resumen del dispositivo

Zfx Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Zfx GmbH - A Company of Zimvie. It received FDA 510(k) clearance on 2024-03-01 under 510(k) number K231915. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the Zfx Abutments?

Zfx Abutments is a medical device that received FDA 510(k) clearance on 2024-03-01. The listed applicant is Zfx GmbH - A Company of Zimvie. The 510(k) number is K231915.

When did Zfx Abutments receive FDA 510(k) clearance?

Zfx Abutments received FDA 510(k) clearance on 2024-03-01, under 510(k) number K231915.

Who is the listed applicant for Zfx Abutments?

The FDA 510(k) record lists Zfx GmbH - A Company of Zimvie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Zfx Abutments?

The FDA product code for Zfx Abutments is NHA.

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Dispositivos relacionados (Código: NHA)

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

K262207Cemented Plus AbutmentUnidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLCK253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, Inc.

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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