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Brilliant Ray Intl., Inc.

United StatesFDA 510(k) applicant, unverified

Devices
7

What Brilliant Ray Intl., Inc. makes

Brilliant Ray Intl., Inc. manufactures patient examination gloves, including latex and non-latex variants sourced from multiple manufacturers in China. The products are designed for single-use medical examinations and procedures, ensuring barrier protection for both patients and healthcare providers.

These devices are classified as Class I under FDA regulations and are listed in the FDA’s 510(k) registry. The company is 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 Brilliant Ray Intl., Inc. have in the registry?

The registry currently lists 7 devices for Brilliant Ray Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Brilliant Ray Intl., Inc.'s devices?

Among its 7 most recently registered devices, Brilliant Ray Intl., Inc. has devices listed in FDA 510(k) (7 devices).

What risk classes do Brilliant Ray Intl., Inc.'s devices fall under?

Among its 7 most recently registered devices, the classes recorded for Brilliant Ray Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Brilliant Ray Intl., Inc. in the registry?

The most recently registered devices listed for Brilliant Ray Intl., Inc. include PATIENT EXAM GLOVES (MFG. XIAN WELFARE LATEX ), PATIENT EXAM GLOVE (LATEX) MFG. TIANJIN JI COUNTY, PATIENT EXAM GLOVES (MFG. CHAGAN TANG CAPITOL) and PATIENT EXAMINATION GLOVES (LATEX).

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