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Universal Bodycare (I) Sdn. Bhd.

MalaysiaFDA 510(k) applicant, unverified

Devices
1

What Universal Bodycare (I) Sdn. Bhd. makes

Universal Bodycare (I) Sdn. Bhd. manufactures NR latex examination gloves, designed for medical and clinical use to reduce the risk of latex allergies during patient examinations.

These products are classified as Class I medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the US.

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

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Universal Bodycare (I) Sdn. Bhd. have in the registry?

The registry currently lists 1 device for Universal Bodycare (I) Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Universal Bodycare (I) Sdn. Bhd.'s devices?

Among its 1 most recently registered device, Universal Bodycare (I) Sdn. Bhd. has devices listed in FDA 510(k) (1 device).

What risk classes do Universal Bodycare (I) Sdn. Bhd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Universal Bodycare (I) Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Universal Bodycare (I) Sdn. Bhd. in the registry?

The most recently registered devices listed for Universal Bodycare (I) Sdn. Bhd. include NR LATEX EXAMINATION GLOVES.

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