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FDA 510(k)

Keymill

K-Number: K172764 · 2018-04-27

ApplicantMycone Dental Supply Company, Inc. (Aka Keystone Industries)
Decision Date2018-04-27
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Keymill is a medical device manufactured by Mycone Dental Supply Company, Inc. (Aka Keystone Industries). It received FDA 510(k) clearance on 2018-04-27 under approval number K172764. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Keymill?

Keymill is a medical device that received FDA 510(k) clearance on 2018-04-27. It is manufactured by Mycone Dental Supply Company, Inc. (Aka Keystone Industries). The 510(k) number is K172764.

When was Keymill approved by the FDA?

Keymill received FDA 510(k) clearance on 2018-04-27, under approval number K172764.

What company makes Keymill?

Keymill is manufactured by Mycone Dental Supply Company, Inc. (Aka Keystone Industries).

What is the FDA product code for Keymill?

The FDA product code for Keymill is EBI.

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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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