FDA applicant

Applied Fiberoptics, Inc.

Southbridge, MA3 decisions1982–19970 recalls

FDA records 3 decisions for Applied Fiberoptics, Inc. (Southbridge, MA) from 1982 to 1997: 3 510(k) clearances. Most are in product codes FGB (Ureteroscope And Accessories, Flexible/Rigid) and EQH (Source, Carrier, Fiberoptic Light). 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 Applied Fiberoptics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Applied Fiberoptics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Applied Fiberoptics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?