Gingi-Aid Gel
K-Number: K211419 · 2022-01-10
ApplicantBelport Company, Inc., Gingi-Pak
Decision Date2022-01-10
Product CodeMVL
DecisionSubstantially Equivalent
Device Summary
Gingi-Aid Gel is a medical device manufactured by Belport Company, Inc., Gingi-Pak. It received FDA 510(k) clearance on 2022-01-10 under approval number K211419. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Gingi-Aid Gel?
Gingi-Aid Gel is a medical device that received FDA 510(k) clearance on 2022-01-10. It is manufactured by Belport Company, Inc., Gingi-Pak. The 510(k) number is K211419.
When was Gingi-Aid Gel approved by the FDA?
Gingi-Aid Gel received FDA 510(k) clearance on 2022-01-10, under approval number K211419.
What company makes Gingi-Aid Gel?
Gingi-Aid Gel is manufactured by Belport Company, Inc., Gingi-Pak.
What is the FDA product code for Gingi-Aid Gel?
The FDA product code for Gingi-Aid Gel is MVL.
Other Devices by Belport Company, Inc., Gingi-Pak
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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.