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Arbor Technologies, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
10

What Arbor Technologies, Inc. makes

Arbor Technologies, Inc. manufactures medical filtration systems and accessories designed for anesthesia, surgical smoke evacuation, and fluid management. Their portfolio includes conduction filters for anesthesia circuits, laser plume filters, syringe filters, and pressure tubing with integrated filtration. The company also produces containment systems for managing hazardous airborne particles during medical procedures, as well as priming devices for intravenous lines.

The company’s devices are classified under FDA regulations as Class I and Class II, with most requiring 510(k) clearance. These products are listed in the FDA’s 510(k) database, reflecting their regulatory status in the United States. The manufacturer is based in the US.

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

Catalogue10

Newest first, rows 1-10 of 10

  • Vacu-Guard Ref K863162

    Not classified
    Active 510(k) 510(k) —

  • Anesthesia Conduction Filter Ref K902666

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

  • Contain(Tm) Ref K895859

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

  • Clyde (Tm) Filtration System Ref K864113

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

  • Autoprime Ref K964283

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

  • Contain(Tm) Laser Plume Filter Ref K902167

    Class I
    Active 510(k) 510(k) I

  • Syringefilter Ref K960928

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

  • Contain(Tm) Ref K874505

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

  • Pressure Tubing And Accessories Ref K922777

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

  • Microsept 60/20 Ref K890844

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

Frequently asked questions

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

The registry currently lists 10 devices for Arbor Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

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

Among its 10 most recently registered devices, Arbor Technologies, Inc. has devices listed in FDA 510(k) (10 devices).

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

Among its 10 most recently registered devices, the classes recorded for Arbor Technologies, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Arbor Technologies, Inc. include VACU-GUARD, ANESTHESIA CONDUCTION FILTER, CONTAIN(TM) and CLYDE (TM) FILTRATION SYSTEM.

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