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 a medical device manufactured by Dental Imaging Technologies Corporation. It received FDA 510(k) clearance on 2026-03-20 under approval 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. It is manufactured by Dental Imaging Technologies Corporation. The 510(k) number is K253864.
When was NOMAD Pro 3 approved by the FDA?
NOMAD Pro 3 received FDA 510(k) clearance on 2026-03-20, under approval number K253864.
What company makes NOMAD Pro 3?
NOMAD Pro 3 is manufactured by Dental Imaging Technologies Corporation.
What is the FDA product code for NOMAD Pro 3?
The FDA product code for NOMAD Pro 3 is EHD.
Other Devices by Dental Imaging Technologies Corporation
Related Devices (Code: EHD)
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.