FDA applicant

Fiberoptic Sensor Technlogies, Inc.

Ann Arbor, MI11 decisions1987–19950 recalls

FDA records 11 decisions for Fiberoptic Sensor Technlogies, Inc. (Ann Arbor, MI) from 1987 to 1995: 11 510(k) clearances. Most are in product codes FEN (Device, Cystometric, Hydraulic) and EXY (Uroflowmeter). 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 Fiberoptic Sensor Technlogies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fiberoptic Sensor Technlogies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Fiberoptic”

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

Fiberoptic Medical Products, Inc. 5 Fiberoptic Fabrications, Inc. 1

Fiberoptic Sensor Technlogies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Fiberoptic”