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FDA 510(k)

MTA vpt

K-Number: K251390 · 2025-07-03

ApplicantVoco GmbH
Decision Date2025-07-03
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MTA vpt is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2025-07-03 under approval number K251390. 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 MTA vpt?

MTA vpt is a medical device that received FDA 510(k) clearance on 2025-07-03. It is manufactured by Voco GmbH. The 510(k) number is K251390.

When was MTA vpt approved by the FDA?

MTA vpt received FDA 510(k) clearance on 2025-07-03, under approval number K251390.

What company makes MTA vpt?

MTA vpt is manufactured by Voco GmbH.

What is the FDA product code for MTA vpt?

The FDA product code for MTA vpt is KIF.

Other Devices by Voco GmbH

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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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