Gingi-Aid Gel
K-Number: K211419 · 2022-01-10
Device Summary
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. The listed applicant is Belport Company, Inc., Gingi-Pak. The 510(k) number is K211419.
When did Gingi-Aid Gel receive FDA 510(k) clearance?
Gingi-Aid Gel received FDA 510(k) clearance on 2022-01-10, under 510(k) number K211419.
Who is the listed applicant for Gingi-Aid Gel?
The FDA 510(k) record lists Belport Company, Inc., Gingi-Pak as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Gingi-Aid Gel?
The FDA product code for Gingi-Aid Gel is MVL.
Other records listing Belport Company, Inc., Gingi-Pak 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: MVL)
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.