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Kelsar Corp.

United StatesFDA applicant, unverified

Devices
2

What Kelsar Corp. makes

Kelsar Corp. manufactures medical devices including urinary drainage bags and enema administration sets.

The company is based in the United States, and its portfolio consists of Class I and Class II devices that are listed in the FDA 510(k) registry.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Urinary Drainage Bag Ref K781987

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Administration Set, Enema Ref K790005

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

Frequently asked questions

How many devices does Kelsar Corp. have in the registry?

The registry currently lists 2 devices for Kelsar Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kelsar Corp.'s devices?

Among its 2 most recently registered devices, Kelsar Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Kelsar Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Kelsar Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Kelsar Corp. in the registry?

The most recently registered devices listed for Kelsar Corp. include URINARY DRAINAGE BAG and ADMINISTRATION SET, ENEMA.

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