FDA 510(k)

Sil-Flow

Número K: K250778 · 2025-05-23

Data da decisão2025-05-23

Código do produtoEBF

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Sil-Flow is the device name listed in this FDA 510(k) record. The listed applicant is Dsi Dental Solutions, Ltd.. It received FDA 510(k) clearance on 2025-05-23 under 510(k) number K250778. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Sil-Flow?

Sil-Flow is a medical device that received FDA 510(k) clearance on 2025-05-23. The listed applicant is Dsi Dental Solutions, Ltd.. The 510(k) number is K250778.

When did Sil-Flow receive FDA 510(k) clearance?

Sil-Flow received FDA 510(k) clearance on 2025-05-23, under 510(k) number K250778.

Who is the listed applicant for Sil-Flow?

The FDA 510(k) record lists Dsi Dental Solutions, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sil-Flow?

The FDA product code for Sil-Flow is EBF.

Outros registros que listam Dsi Dental Solutions, Ltd. como candidato(a)

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

K200188DSI Dental Implant System

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Fonte oficial

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