TrusFIL-Flow Flowable Composite Restorative
K-Number: K221510 · 2022-10-12
Device Summary
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. The listed applicant is Rizhao Huge Biomaterials Company, Ltd.. The 510(k) number is K221510.
When did TrusFIL-Flow Flowable Composite Restorative receive FDA 510(k) clearance?
TrusFIL-Flow Flowable Composite Restorative received FDA 510(k) clearance on 2022-10-12, under 510(k) number K221510.
Who is the listed applicant for TrusFIL-Flow Flowable Composite Restorative?
The FDA 510(k) record lists Rizhao Huge Biomaterials Company, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TrusFIL-Flow Flowable Composite Restorative?
The FDA product code for TrusFIL-Flow Flowable Composite Restorative is EBF.
Related Clinical Trials
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.
Other records listing Rizhao Huge Biomaterials Company, 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.
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.
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.