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Transmotion Medical, Inc.

Country not established

Devices
1
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Transmotion Medical, Inc. makes

Transmotion Medical, Inc. manufactures power drive chairs designed for mobility assistance, including the TMM6 model, which supports patient transfer and positioning in clinical or home care settings.

The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

FDA recalls1

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

FDA recall records list 1 recall initiated by Transmotion Medical, Inc., initiated on 2014-11-14. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. 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.

  • 2014

    • 14 Nov 2014 Z-0996-2015 Class II Terminated The firm is finding that the stretcher chair controllers are moving the chairs involuntarily. Distribution: Worldwide Distribution - US Distribution and the countries including Canada, Australia, Chile, China, Costa Rica,…
      Full distribution text Worldwide Distribution - US Distribution and the countries including Canada, Australia, Chile, China, Costa Rica, Germany, Algeria, Israel, Italy, South Korea, Malaysia, Nigeria, Netherlands, Poland, Portugal, Saudi Arabia, Singapore, Thailand, and Venezuela.

Frequently asked questions

How many devices does Transmotion Medical, Inc. have in the registry?

The registry currently lists 1 device for Transmotion Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Transmotion Medical, Inc.'s devices?

Among its 1 most recently registered device, Transmotion Medical, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Transmotion Medical, Inc.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Transmotion Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Transmotion Medical, Inc.?

FDA recall records list 1 recall initiated by Transmotion Medical, Inc., the most recent initiated on 14 Nov 2014. 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 Transmotion Medical, Inc. in the registry?

The most recently registered devices listed for Transmotion Medical, Inc. include POWER DRIVE CHAIR, MODEL: TMM6.

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