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FDA 510(k)

TrusFIL-Flow Flowable Composite Restorative

K-Number: K221510 · 2022-10-12

Decision Date2022-10-12
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TrusFIL-Flow Flowable Composite Restorative is a medical device manufactured by Rizhao Huge Biomaterials Company, Ltd.. It received FDA 510(k) clearance on 2022-10-12 under approval number K221510. 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 TrusFIL-Flow Flowable Composite Restorative?

TrusFIL-Flow Flowable Composite Restorative is a medical device that received FDA 510(k) clearance on 2022-10-12. It is manufactured by Rizhao Huge Biomaterials Company, Ltd.. The 510(k) number is K221510.

When was TrusFIL-Flow Flowable Composite Restorative approved by the FDA?

TrusFIL-Flow Flowable Composite Restorative received FDA 510(k) clearance on 2022-10-12, under approval number K221510.

What company makes TrusFIL-Flow Flowable Composite Restorative?

TrusFIL-Flow Flowable Composite Restorative is manufactured by Rizhao Huge Biomaterials Company, Ltd..

What is the FDA product code for TrusFIL-Flow Flowable Composite Restorative?

The FDA product code for TrusFIL-Flow Flowable Composite Restorative is EBF.

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Official Source

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