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Golden Vision, Inc.

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Devices
1

What Golden Vision, Inc. makes

Golden Vision, Inc. manufactures the Goldman Manual Tonometer, a handheld device used for measuring intraocular pressure in the eye to assess glaucoma risk and monitor ocular health.

The Goldman Manual Tonometer is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) clearance process. 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

  • Goldman Manual Tonometer Ref K981432

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

Frequently asked questions

How many devices does Golden Vision, Inc. have in the registry?

The registry currently lists 1 device for Golden Vision, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Golden Vision, Inc.'s devices?

Among its 1 most recently registered device, Golden Vision, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Golden Vision, Inc.'s devices fall under?

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

What are the newest devices from Golden Vision, Inc. in the registry?

The most recently registered devices listed for Golden Vision, Inc. include GOLDMAN MANUAL TONOMETER.

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