FDA applicant

Cogent Light Technologies, Inc.

Valencia, CA5 decisions1994–20000 recalls

FDA records 5 decisions for Cogent Light Technologies, Inc. (Valencia, CA) from 1994 to 2000: 5 510(k) clearances. Most are in product codes GCT (Light Source, Endoscope, Xenon Arc) and FFS (Image, Illumination, Fiberoptic, For Endoscope). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Cogent Light Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cogent Light Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cogent Light Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Cogent”

FDA records each applicant name separately; these may or may not be the same firm.

Cogent Diagnotics, Ltd. 31 Cogent Spine, LLC 3 Cogent Therapeutics, LLC 1 Cogent 1

Cogent Light Technologies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cogent”