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FDA 510(k)

Velmeni for Dentists (V4D)

K-Number: K240003 · 2024-08-30

ApplicantVelmeni, Inc.
Decision Date2024-08-30
Product CodeMYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Velmeni for Dentists (V4D) is a medical device manufactured by Velmeni, Inc.. It received FDA 510(k) clearance on 2024-08-30 under approval number K240003. The device is classified under product code MYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Velmeni for Dentists (V4D)?

Velmeni for Dentists (V4D) is a medical device that received FDA 510(k) clearance on 2024-08-30. It is manufactured by Velmeni, Inc.. The 510(k) number is K240003.

When was Velmeni for Dentists (V4D) approved by the FDA?

Velmeni for Dentists (V4D) received FDA 510(k) clearance on 2024-08-30, under approval number K240003.

What company makes Velmeni for Dentists (V4D)?

Velmeni for Dentists (V4D) is manufactured by Velmeni, Inc..

What is the FDA product code for Velmeni for Dentists (V4D)?

The FDA product code for Velmeni for Dentists (V4D) is MYN.

Other Devices by Velmeni, Inc.

K250753VELMENI for DENTISTS (V4D) K252953Velmeni for Dentists (V4D) Endo-Perio

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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.

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