Contour Light (CL-100)
K-Number: K243854 · 2026-02-13
Device Summary
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. The listed applicant is Contour Research, LLC. The 510(k) number is K243854.
When did Contour Light (CL-100) receive FDA 510(k) clearance?
Contour Light (CL-100) received FDA 510(k) clearance on 2026-02-13, under 510(k) number K243854.
Who is the listed applicant for Contour Light (CL-100)?
The FDA 510(k) record lists Contour Research, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Contour Light (CL-100)?
The FDA product code for Contour Light (CL-100) is OLI.
Other records listing Contour Research, LLC 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: OLI)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.