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Tridak Division of Indicon, Inc.

United StatesFDA applicant, unverified

Devices
7

What Tridak Division of Indicon, Inc. makes

Tridak Division of Indicon, Inc. manufactures fiberoptic-based medical devices, including pressure sensors and light cables for diagnostic and surgical applications. Their portfolio also includes ophthalmic surgical instruments, urodynamic processing systems for bladder function analysis, and a multi-spatula device for cervical cytology sampling. Additionally, they produce a non-implanted electrical continence device for urinary control.

The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) clearance database. Their products are listed under U.S. regulatory authorities, and the division operates as part of Indicon, Inc., based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Tridak Division of Indicon, Inc. have in the registry?

The registry currently lists 7 devices for Tridak Division of Indicon, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tridak Division of Indicon, Inc.'s devices?

Among its 7 most recently registered devices, Tridak Division of Indicon, Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Tridak Division of Indicon, Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Tridak Division of Indicon, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Tridak Division of Indicon, Inc. in the registry?

The most recently registered devices listed for Tridak Division of Indicon, Inc. include LABORIE FIBEROPTIC PRESSURE SENSOR & INTERFACE, LABORIE FIBREOPTIC LIGHT CABLE, OPTHALMIC SURGICAL INSTRUMENTS and NONIMPLANTED ELECTRICAL CONTINENCE DEVICE.

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