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Paraflex Corp.

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Devices
1

What Paraflex Corp. makes

Paraflex Corp. manufactures ROMFLEX, which is a Class I medical device.

The company is based in the US and its devices are listed in the FDA 510(k) registry.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Romflex Ref K905718

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

Frequently asked questions

How many devices does Paraflex Corp. have in the registry?

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

Which registries list Paraflex Corp.'s devices?

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

What risk classes do Paraflex Corp.'s devices fall under?

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

What are the newest devices from Paraflex Corp. in the registry?

The most recently registered devices listed for Paraflex Corp. include ROMFLEX.

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