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FDA 510(k)

Sil-Flow

K-Number: K250778 · 2025-05-23

ApplicantDsi Dental Solutions, Ltd.
Decision Date2025-05-23
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

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.

Frequently Asked Questions

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.

Other records listing Dsi Dental Solutions, Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K200188DSI Dental Implant System

Related Devices (Code: EBF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K261246SRGC-06GC America, Inc.K261093DIAFILDiaDent Group InternationalK261071DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)DiaDent Group InternationalK260805Dual CoreVericom Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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