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FDA 510(k)

Injectable Root Canal Bioceramic Sealer

K-Number: K212983 · 2021-12-08

Decision Date2021-12-08
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Injectable Root Canal Bioceramic Sealer is a medical device manufactured by Beijing C-Root Dental Medical Devices Co., Ltd.. It received FDA 510(k) clearance on 2021-12-08 under approval number K212983. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Injectable Root Canal Bioceramic Sealer?

Injectable Root Canal Bioceramic Sealer is a medical device that received FDA 510(k) clearance on 2021-12-08. It is manufactured by Beijing C-Root Dental Medical Devices Co., Ltd.. The 510(k) number is K212983.

When was Injectable Root Canal Bioceramic Sealer approved by the FDA?

Injectable Root Canal Bioceramic Sealer received FDA 510(k) clearance on 2021-12-08, under approval number K212983.

What company makes Injectable Root Canal Bioceramic Sealer?

Injectable Root Canal Bioceramic Sealer is manufactured by Beijing C-Root Dental Medical Devices Co., Ltd..

What is the FDA product code for Injectable Root Canal Bioceramic Sealer?

The FDA product code for Injectable Root Canal Bioceramic Sealer is KIF.

Related Clinical Trials

Other Devices by Beijing C-Root Dental Medical Devices Co., Ltd.

Related Devices (Code: KIF)

Official Source

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