FDA applicant

Fiberoptics Technology, Inc.

Pomfret, CT2 decisions1991–20100 recalls

FDA records 2 decisions for Fiberoptics Technology, Inc. (Pomfret, CT) from 1991 to 2010: 2 510(k) clearances. Most are in product codes NTN (Led Light Source) and EQH (Source, Carrier, Fiberoptic Light). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Fiberoptics Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

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Fiberoptics Technology, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?