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FDA 510(k)

NOMAD Pro 3

K-Number: K253864 · 2026-03-20

Decision Date2026-03-20
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NOMAD Pro 3 is the device name listed in this FDA 510(k) record. The listed applicant is Dental Imaging Technologies Corporation. It received FDA 510(k) clearance on 2026-03-20 under 510(k) number K253864. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOMAD Pro 3?

NOMAD Pro 3 is a medical device that received FDA 510(k) clearance on 2026-03-20. The listed applicant is Dental Imaging Technologies Corporation. The 510(k) number is K253864.

When did NOMAD Pro 3 receive FDA 510(k) clearance?

NOMAD Pro 3 received FDA 510(k) clearance on 2026-03-20, under 510(k) number K253864.

Who is the listed applicant for NOMAD Pro 3?

The FDA 510(k) record lists Dental Imaging Technologies Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NOMAD Pro 3?

The FDA product code for NOMAD Pro 3 is EHD.

Other records listing Dental Imaging Technologies Corporation 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.

Related Devices (Code: EHD)

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.