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Prosben, Inc.

TaiwanFDA applicant, unverified FDA FEI 3005668459

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Prosben, Inc. makes

Prosben, Inc. manufactures contact lens cases, specifically the CA66-02, CA66-03WB, and CA66-04T series.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 29 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3005668459
Address
8F., No. 58, Sec. 3, TAIPEI CITY

Frequently asked questions

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

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

Which registries list Prosben, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Prosben, Inc. include PROSBEN CONTACT LENS CASES MODEL CA66-02, CA66-03WB, CA66-04T SERIES.

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