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FDA 510(k)

Titan Dental Design

K-Number: K232429 · 2023-10-13

Decision Date2023-10-13
Product CodePNN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Titan Dental Design is the device name listed in this FDA 510(k) record. The listed applicant is Clearadvance, LLC. It received FDA 510(k) clearance on 2023-10-13 under 510(k) number K232429. The device is classified under product code PNN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Titan Dental Design?

Titan Dental Design is a medical device that received FDA 510(k) clearance on 2023-10-13. The listed applicant is Clearadvance, LLC. The 510(k) number is K232429.

When did Titan Dental Design receive FDA 510(k) clearance?

Titan Dental Design received FDA 510(k) clearance on 2023-10-13, under 510(k) number K232429.

Who is the listed applicant for Titan Dental Design?

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

What is the FDA product code for Titan Dental Design?

The FDA product code for Titan Dental Design is PNN.

Related Devices (Code: PNN)

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.

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.