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Baron Technologies, Inc.

United StatesFDA applicant, unverified

Devices
2

What Baron Technologies, Inc. makes

Baron Technologies, Inc. manufactures intravascular catheters and hypodermic syringes, designed for medical procedures requiring precise fluid administration or vascular access.

These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Bt Cath (Intravascular Catheter) Ref K862480

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Bt Hypodermic Syringe Ref K864541

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

Frequently asked questions

How many devices does Baron Technologies, Inc. have in the registry?

The registry currently lists 2 devices for Baron Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Baron Technologies, Inc.'s devices?

Among its 2 most recently registered devices, Baron Technologies, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Baron Technologies, Inc.'s devices fall under?

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

What are the newest devices from Baron Technologies, Inc. in the registry?

The most recently registered devices listed for Baron Technologies, Inc. include BT CATH (INTRAVASCULAR CATHETER) and BT HYPODERMIC SYRINGE.

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