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FDA 510(k)

DentureID Microchip

K-Number: K170423 · 2017-10-25

ApplicantCmp Industries, LLC
Decision Date2017-10-25
Product CodePYQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DentureID Microchip is the device name listed in this FDA 510(k) record. The listed applicant is Cmp Industries, LLC. It received FDA 510(k) clearance on 2017-10-25 under 510(k) number K170423. The device is classified under product code PYQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DentureID Microchip?

DentureID Microchip is a medical device that received FDA 510(k) clearance on 2017-10-25. The listed applicant is Cmp Industries, LLC. The 510(k) number is K170423.

When did DentureID Microchip receive FDA 510(k) clearance?

DentureID Microchip received FDA 510(k) clearance on 2017-10-25, under 510(k) number K170423.

Who is the listed applicant for DentureID Microchip?

The FDA 510(k) record lists Cmp Industries, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DentureID Microchip?

The FDA product code for DentureID Microchip is PYQ.

Other records listing Cmp Industries, LLC 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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