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Shineo Technology Co., Ltd.

TaiwanFDA applicant, unverified FDA FEI 3043503913

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Shineo Technology Co., Ltd. makes

Shineo Technology Co., Ltd. manufactures silicone implants, specifically the ShiNeo Silicone Implant, which is a medical device designed for implantation in the body.

The ShiNeo Silicone Implant is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • ShiNeo Silicone Implant Ref K222748

    Active Regimes: 510(k) Registry: 510(k) Class:II

Company details

FDA FEI number
3043503913
Address
5F., No.207-4, Xinshu Rd., New Taipei City

Frequently asked questions

How many devices does Shineo Technology Co., Ltd. have in the registry?

The registry currently lists 1 device for Shineo Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shineo Technology Co., Ltd.'s devices?

Among its 1 most recently registered device, Shineo Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Shineo Technology Co., Ltd.'s devices fall under?

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

What are the newest devices from Shineo Technology Co., Ltd. in the registry?

The most recently registered devices listed for Shineo Technology Co., Ltd. include ShiNeo Silicone Implant.

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