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 the device name listed in this FDA 510(k) record. The listed applicant is Mycone Dental Supply Company, Inc. (Aka Keystone Industries). It received FDA 510(k) clearance on 2018-04-27 under 510(k) 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. The listed applicant is Mycone Dental Supply Company, Inc. (Aka Keystone Industries). The 510(k) number is K172764.

When did Keymill receive FDA 510(k) clearance?

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

Who is the listed applicant for Keymill?

The FDA 510(k) record lists Mycone Dental Supply Company, Inc. (Aka Keystone Industries) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Keymill?

The FDA product code for Keymill is EBI.

Related Devices (Code: EBI)

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.

K261626UltraPrint Flexible Denture UVGuangzhou Heygears IMC., Inc.K262681NanoCeram Resin3BFAB TEKNOLOJI A.S.K262300Denture Base Resin V2Formlabs Ohio, Inc.K261474DENTCA Tru FlexibleDentca, Inc.K260569DB 4000 High Impact Denture BaseCarbon, Inc.K260376Denture BaseShandong Huge Dental Material Corporation

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.