FDA 510(k)

The POD

K-Number: K182820 · 2019-07-17

Decision Date2019-07-17

Product CodeMQC

DecisionSubstantially Equivalent

Device Summary

The POD is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Facialdontics, LLC. It received FDA 510(k) clearance on 2019-07-17 under 510(k) number K182820. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the The POD?

The POD is a medical device that received FDA 510(k) clearance on 2019-07-17. The listed applicant is Advanced Facialdontics, LLC. The 510(k) number is K182820.

When did The POD receive FDA 510(k) clearance?

The POD received FDA 510(k) clearance on 2019-07-17, under 510(k) number K182820.

Who is the listed applicant for The POD?

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

What is the FDA product code for The POD?

The FDA product code for The POD is MQC.

Other records listing Advanced Facialdontics, 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.