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K-Seven Industries, Inc.

Country not established

Devices
1

What K-Seven Industries, Inc. makes

K-Seven Industries, Inc. manufactures sterile storage containers designed to hold and protect medical devices, implants, or surgical instruments during sterilization and storage. These containers are engineered to maintain sterility and prevent contamination while ensuring compatibility with common sterilization methods.

The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway in the United States. The portfolio is regulated under the FDA’s medical device authorization framework, with compliance requirements aligned with U.S. regulatory standards.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Steristorage Container Ref K853450

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does K-Seven Industries, Inc. have in the registry?

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

Which registries list K-Seven Industries, Inc.'s devices?

Among its 1 most recently registered device, K-Seven Industries, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do K-Seven Industries, Inc.'s devices fall under?

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

What are the newest devices from K-Seven Industries, Inc. in the registry?

The most recently registered devices listed for K-Seven Industries, Inc. include STERISTORAGE CONTAINER.

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