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Saxnor Corp.

United StatesFDA applicant, unverified

Devices
2

What Saxnor Corp. makes

Saxnor Corp. manufactures intravenous (I.V.) filter holders, including models compatible with Frehan Inc. systems. These devices are designed to secure and stabilize I.V. filters during use, reducing the risk of dislodgement or contamination in fluid administration.

The company’s products fall under FDA Class I medical devices and are listed via the 510(k) pathway. The portfolio is regulated under U.S. FDA standards, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • I.V. Filter Holder Ref K832300

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Frehan Inc. I.V. Filter Holder Ref K830300

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

Frequently asked questions

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

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

Which registries list Saxnor Corp.'s devices?

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

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

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

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

The most recently registered devices listed for Saxnor Corp. include I.V. FILTER HOLDER and FREHAN INC. I.V. FILTER HOLDER.

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