Injectable Root Canal Bioceramic Sealer
K-Number: K212983 · 2021-12-08
Device Summary
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.
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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.