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Novacon Corp.

United StatesFDA applicant, unverified

Devices
6

What Novacon Corp. makes

Novacon Corp. manufactures infusion pumps designed for diabetes management, including disposable insulin infusion devices and a reusable system for continuous subcutaneous insulin delivery.

The company’s products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue6

Newest first, rows 1-6 of 6

  • Dib Infusors Ref K944665

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Freedom Infusion System Ref K992015

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Dib Infusor-Ra Ref K960318

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Dib Infusor Ref K941766

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Dib Infusor Ref K930404

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Dib Infusor Ref K955849

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

Frequently asked questions

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

The registry currently lists 6 devices for Novacon Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Novacon Corp.'s devices?

Among its 6 most recently registered devices, Novacon Corp. has devices listed in FDA 510(k) (6 devices).

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

Among its 6 most recently registered devices, the classes recorded for Novacon Corp.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Novacon Corp. include DIB INFUSORS, FREEDOM INFUSION SYSTEM, DIB INFUSOR-RA and DIB INFUSOR.

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