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Life Technology

Country not established

Devices
1

What Life Technology makes

Life Technology manufactures the DOCUMENTOR, a device designed for capturing and archiving medical documentation, likely in a clinical or procedural setting to ensure record-keeping compliance and accessibility.

The DOCUMENTOR is classified as a Class II medical device under FDA regulations and is authorised via 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Documentor Ref K842715

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

Frequently asked questions

How many devices does Life Technology have in the registry?

The registry currently lists 1 device for Life Technology. Devices recorded under merged duplicate company entries are counted once.

Which registries list Life Technology's devices?

Among its 1 most recently registered device, Life Technology has devices listed in FDA 510(k) (1 device).

What risk classes do Life Technology's devices fall under?

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

What are the newest devices from Life Technology in the registry?

The most recently registered devices listed for Life Technology include DOCUMENTOR.

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