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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 the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2025-07-03 under 510(k) 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. The listed applicant is Voco GmbH. The 510(k) number is K251390.

When did MTA vpt receive FDA 510(k) clearance?

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

Who is the listed applicant for MTA vpt?

The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MTA vpt?

The FDA product code for MTA vpt is KIF.

Other records listing Voco GmbH 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.

K252073VOCO Profluorid Varnish + BioMinK261357Grandio disc multicolorK252606Bifix Veneer LC, Bifix Veneer Try-InK251239GrandioSO UnlimitedK231817AlignerFlow LCK231591V-Print c&b temp

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Related Devices (Code: KIF)

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.

K261415Injectable Root Canal Sealer (KP-Root SP)Guilin Kevin Peter Technology Co., Ltd.K253167Any-PasteMediclus Co., Ltd.K252890ZenSeal ProKerr CorporationK251465Root canal repair materials (nRoot BP)Enpuno Biotechnology Co., Ltd.K252285Well-Root PTVericom Co., Ltd.K251884One-Fil Putty InjectableMediclus Co., Ltd.

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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