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FDA 510(k)

Contour Light (CL-100)

K-Number: K243854 · 2026-02-13

Decision Date2026-02-13
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Contour Light (CL-100) is a medical device manufactured by Contour Research, LLC. It received FDA 510(k) clearance on 2026-02-13 under approval number K243854. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Contour Light (CL-100)?

Contour Light (CL-100) is a medical device that received FDA 510(k) clearance on 2026-02-13. It is manufactured by Contour Research, LLC. The 510(k) number is K243854.

When was Contour Light (CL-100) approved by the FDA?

Contour Light (CL-100) received FDA 510(k) clearance on 2026-02-13, under approval number K243854.

What company makes Contour Light (CL-100)?

Contour Light (CL-100) is manufactured by Contour Research, LLC.

What is the FDA product code for Contour Light (CL-100)?

The FDA product code for Contour Light (CL-100) is OLI.

Other Devices by Contour Research, LLC

Related Devices (Code: OLI)

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.