Skip to content

Glovmaster Sdn. Bhd.

MalaysiaFDA applicant, unverified FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Glovmaster Sdn. Bhd. makes

Glovmaster Sdn. Bhd. manufactures powder-free nitrile examination gloves, designed for medical and clinical use to reduce allergic reactions and skin irritation.

The company’s products fall under FDA Class I devices and are listed via 510(k) clearance in the United States. The manufacturer 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

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Glovmaster Sdn. Bhd BANTING Selangor · MY FEI 3022538552

Frequently asked questions

How many devices does Glovmaster Sdn. Bhd. have in the registry?

The registry currently lists 1 device for Glovmaster Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Glovmaster Sdn. Bhd.'s devices?

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

What risk classes do Glovmaster Sdn. Bhd.'s devices fall under?

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

What are the newest devices from Glovmaster Sdn. Bhd. in the registry?

The most recently registered devices listed for Glovmaster Sdn. Bhd. include Glovmaster Nitrile Examination Glove Powder Free.

Which FDA establishments are linked to Glovmaster Sdn. Bhd.?

1 FDA establishment is linked to Glovmaster Sdn. Bhd. in the registry; they are listed on the company page.

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