FDA 510(k)

Oryx Cloud Imaging

K-Number: K220684 · 2022-04-29

Decision Date2022-04-29

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Oryx Cloud Imaging is the device name listed in this FDA 510(k) record. The listed applicant is Oryx Dental Software, Inc.. It received FDA 510(k) clearance on 2022-04-29 under 510(k) number K220684. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Oryx Cloud Imaging?

Oryx Cloud Imaging is a medical device that received FDA 510(k) clearance on 2022-04-29. The listed applicant is Oryx Dental Software, Inc.. The 510(k) number is K220684.

When did Oryx Cloud Imaging receive FDA 510(k) clearance?

Oryx Cloud Imaging received FDA 510(k) clearance on 2022-04-29, under 510(k) number K220684.

Who is the listed applicant for Oryx Cloud Imaging?

The FDA 510(k) record lists Oryx Dental Software, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Oryx Cloud Imaging?

The FDA product code for Oryx Cloud Imaging is LLZ.

Related Devices (Code: LLZ)

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.