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FDA 510(k)

Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT)

K-Number: K260152 · 2026-04-23

ApplicantMmtech Projetos Tecnologicos Importacao E Exportacao Ltda.
Decision Date2026-04-23
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT) is the device name listed in this FDA 510(k) record. The listed applicant is Mmtech Projetos Tecnologicos Importacao E Exportacao Ltda.. It received FDA 510(k) clearance on 2026-04-23 under 510(k) number K260152. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT)?

Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT) is a medical device that received FDA 510(k) clearance on 2026-04-23. The listed applicant is Mmtech Projetos Tecnologicos Importacao E Exportacao Ltda.. The 510(k) number is K260152.

When did Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT) receive FDA 510(k) clearance?

Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT) received FDA 510(k) clearance on 2026-04-23, under 510(k) number K260152.

Who is the listed applicant for Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT)?

The FDA 510(k) record lists Mmtech Projetos Tecnologicos Importacao E Exportacao Ltda. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT)?

The FDA product code for Smart Print Bio Vitality (A2, A3, BL1, B1, A2-HT, A3-HT, BL1-HT, B1-HT) is EBF.

Related Devices (Code: EBF)

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.

K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K261246SRGC-06GC America, Inc.K261093DIAFILDiaDent Group InternationalK261071DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW (0.5g)DiaDent Group InternationalK260805Dual CoreVericom 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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