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Independence Technology, LLC

Country not established

Devices
2
FDA recalls
3

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Independence Technology, LLC makes

Independence Technology, LLC manufactures manual assist wheelchairs and powered mobility systems, including the IGLIDE Manual Assist Wheelchair and the Independence iBOT 3000/4000 Mobility System. These devices are designed to enhance mobility for users with limited mobility, offering both manual and motorized options for independent movement.

The company’s products are regulated as Class II medical devices in the US, with some models authorised via the FDA’s 510(k) and PMA pathways. The devices are listed under the FDA’s regulatory framework and comply with applicable US medical device standards.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

FDA recalls3

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 3 recalls initiated by Independence Technology, LLC, the earliest on 2004-07-01 and the most recent on 2010-02-22. By recorded status: 3 terminated. The reasons filed fall into these groups: electrical or power and mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2010

    • 22 Feb 2010 Z-1775-2010 Unclassified (pre-2012) Terminated A thermal breaker in the battery pack has the potential to open due to overheating and disable one third of the cells in the affected battery pack. Distribution: Nationwide and to the United Kingdom. Submission number: P020033

  • 2004

    • 30 Aug 2004 Z-0022-05 Unclassified (pre-2012) Terminated Rocks and debris can enter into the wheel cluster housing through a damaged wheel cap causing wheel malfunction. Distribution: The Independence IBOT 3000 Mobility System was distributed to direct customers in the US, the UK, Ireland, and New…
      Full distribution text The Independence IBOT 3000 Mobility System was distributed to direct customers in the US, the UK, Ireland, and New Zealand. Ten of the US Direct customers received their devices via the VA. One training/demo/assessment device was distributed to the firm''s European support Centre (Ortho Clinical Diagnostics) in France. Two training/demo/assessment devices were distributed to a J&J representative in Japan.
      Submission number: P020033
    • 1 Jul 2004 Z-1383-04 Unclassified (pre-2012) Terminated iBOT Mobility System may tip over due to malfunction in power base. Distribution: The Independence iBOT 3000 Mobility System was distributed to direct customers in the US, the UK, Ireland, and New…
      Full distribution text The Independence iBOT 3000 Mobility System was distributed to direct customers in the US, the UK, Ireland, and New Zealand. Ten of the US Direct customers received their devices via the VA. One traning/demo/assessment device was distributed to the firm''s European Support Centre (Ortho Clinical Diagnostics) in France. Two training/demo/assessment devices were distributed to a J&J representative in Japan.
      Submission number: P020033

Frequently asked questions

How many devices does Independence Technology, LLC have in the registry?

The registry currently lists 2 devices for Independence Technology, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list Independence Technology, LLC's devices?

Among its 2 most recently registered devices, Independence Technology, LLC has devices listed in FDA 510(k) (1 device) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Independence Technology, LLC's devices fall under?

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

Are there FDA recall records for Independence Technology, LLC?

FDA recall records list 3 recalls initiated by Independence Technology, LLC, the most recent initiated on 22 Feb 2010. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Independence Technology, LLC in the registry?

The most recently registered devices listed for Independence Technology, LLC include IGLIDE MANUAL ASSIST WHEELCHAIR and INDEPENDENCE (TM) IBOT 3000/4000 MOBILITY SYSTEM.

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