Data / Medical devices / United States / C. Light Technologies, Inc.

C. Light Technologies, Inc.: FDA-registered device maker in Santa Clara, CA, United States, 1 510(k) clearance

C. Light Technologies, Inc. is registered with the FDA (registration 3027593072) in Santa Clara, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 9, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3027593072

Address

1700 Wyatt Dr. Suite 6, Santa Clara, CA, United States, 95054

Owner or operator

C. Light Technologies, Inc. (10088349)

Roles

Complaint file establishment, Manufacturer, Specification developer

First device listed

July 5, 2023

Registered through

2026

Brand names listed

Retitrack

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Updated May 9, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.