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P L Overseas Limited

Hong Kong SAR ChinaFDA 510(k) applicant, unverified FDA FEI 3014254835

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What P L Overseas Limited makes

P L Overseas Limited manufactures contact lens cases, including models A-1 and B-1, designed for storing and maintaining single-use contact lenses.

These products are classified as Class II devices under US regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3014254835
Address
FLAT / RM 1101 BLK 1 11F, CHEUNG SHA WAN PLAZA,, HONG KONG

Frequently asked questions

How many devices does P L Overseas Limited have in the registry?

The registry currently lists 1 device for P L Overseas Limited. Devices recorded under merged duplicate company entries are counted once.

Which registries list P L Overseas Limited's devices?

Among its 1 most recently registered device, P L Overseas Limited has devices listed in FDA 510(k) (1 device).

What risk classes do P L Overseas Limited's devices fall under?

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

What are the newest devices from P L Overseas Limited in the registry?

The most recently registered devices listed for P L Overseas Limited include Contact Lens Case, Model: A-1, B-1.

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