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Tiolat Oy

Country not established

Devices
1

What Tiolat Oy makes

Tiolat OY manufactures the ICARE TONOMETER TA01I, a non-contact tonometer used for measuring intraocular pressure in the eye to aid in the diagnosis and monitoring of glaucoma.

The ICARE TONOMETER TA01I is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Icare Tonometer TA01I Ref K063873

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Tiolat OY have in the registry?

The registry currently lists 1 device for Tiolat OY. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tiolat OY's devices?

Among its 1 most recently registered device, Tiolat OY has devices listed in FDA 510(k) (1 device).

What risk classes do Tiolat OY's devices fall under?

Among its 1 most recently registered device, the classes recorded for Tiolat OY's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Tiolat OY in the registry?

The most recently registered devices listed for Tiolat OY include ICARE TONOMETER TA01I.

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