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Fiberoptic Sensor Technlogies, Inc.

United StatesFDA applicant, unverified

Devices
11

What Fiberoptic Sensor Technlogies, Inc. makes

Fiberoptic Sensor Technologies, Inc. manufactures disposable and reusable fiber optic transducers, urodynamic catheters, and pressure monitoring systems for urological assessments. Their products include single and dual-pressure catheters, urodynamic monitoring devices, and catheter introducer systems designed for measuring bladder and urethral pressures. The company also supplies fiber optic pressure converters and specialized Foley catheters with fiberoptic tips for clinical use.

The company’s portfolio consists of Class II medical devices, regulated under the FDA’s 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, ensuring compliance with U.S. medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Fiberoptic Sensor Technlogies, Inc. have in the registry?

The registry currently lists 11 devices for Fiberoptic Sensor Technlogies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Fiberoptic Sensor Technlogies, Inc.'s devices?

Among its 11 most recently registered devices, Fiberoptic Sensor Technlogies, Inc. has devices listed in FDA 510(k) (11 devices).

What risk classes do Fiberoptic Sensor Technlogies, Inc.'s devices fall under?

Among its 11 most recently registered devices, the classes recorded for Fiberoptic Sensor Technlogies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Fiberoptic Sensor Technlogies, Inc. in the registry?

The most recently registered devices listed for Fiberoptic Sensor Technlogies, Inc. include FST DISPOSABLE FIBER OPTIC TRANSDUCER #0100-00, FST CATH-UD, CATHETER, URO-PRO 2000 and FST CATH UD-DUAL DUAL PRESSURE CATHETER.

Generated automatically from registry data and not verified by a human reviewer.