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CnS Medical Co., Ltd.

South KoreaFDA applicant, unverified FDA FEI 3021519357

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What CnS Medical Co., Ltd. makes

CnS Medical Co., Ltd. manufactures the DELPHI System, a medical device designed for [specific clinical application not detailed in provided data].

The DELPHI System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. 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

  • DELPHI System Ref K242907

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

Company details

FDA FEI number
3021519357
Address
94-40 Yongjeonggyeongje-ro 1-gil, Gunnae-myeon, Pocheon-si, Gyeonggi-do, Republic of Korea, Pocheon-si Gyeonggi

Frequently asked questions

How many devices does CnS Medical Co., Ltd. have in the registry?

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

Which registries list CnS Medical Co., Ltd.'s devices?

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

What risk classes do CnS Medical Co., Ltd.'s devices fall under?

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

What are the newest devices from CnS Medical Co., Ltd. in the registry?

The most recently registered devices listed for CnS Medical Co., Ltd. include DELPHI System.

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