Grandio disc multicolor
K-Number: K261357 · 2026-04-27
ApplicantVoco GmbH
Decision Date2026-04-27
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Grandio disc multicolor is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2026-04-27 under approval number K261357. 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 Grandio disc multicolor?
Grandio disc multicolor is a medical device that received FDA 510(k) clearance on 2026-04-27. It is manufactured by Voco GmbH. The 510(k) number is K261357.
When was Grandio disc multicolor approved by the FDA?
Grandio disc multicolor received FDA 510(k) clearance on 2026-04-27, under approval number K261357.
What company makes Grandio disc multicolor?
Grandio disc multicolor is manufactured by Voco GmbH.
What is the FDA product code for Grandio disc multicolor?
The FDA product code for Grandio disc multicolor is EBF.
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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.