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Zibo Shengkun Chemical Industry Co Ltd

Country not established FDA establishment FEI 3009218271

Devices
1
Registrations
FDA
FDA recalls
0

What Zibo Shengkun Chemical Industry Co Ltd makes

ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD manufactures Powder Free Polyurethane Examination Gloves (Pink).

The company's products are listed in the FDA 510(k) registry and are classified as Class I medical devices. The company is based in China.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3009218271
Address
Lot 6, No. 21 Qingtian Road, Zibo Shandong

FDA establishments1

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

  • Zibo Shengkun Chemical Industry Co., Ltd. US

Frequently asked questions

How many devices does ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD have in the registry?

The registry currently lists 1 device for ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD. Devices recorded under merged duplicate company entries are counted once.

Which registries list ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD's devices?

Among its 1 most recently registered device, ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD has devices listed in FDA 510(k) (1 device).

What risk classes do ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD's devices fall under?

Among its 1 most recently registered device, the classes recorded for ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD in the registry?

The most recently registered devices listed for ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD include Powder Free Polyurethane Examination Gloves (Pink).

Which FDA establishments are linked to ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD?

1 FDA establishment is linked to ZIBO SHENGKUN CHEMICAL INDUSTRY CO LTD in the registry; they are listed on the company page.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.