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Bioflex, Inc.

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Devices
1

What Bioflex, Inc. makes

Bioflex, Inc. manufactures custom-fitted Bioflex Garments designed for medical compression and patient immobilization, including models for post-surgical recovery, wound care, and orthopedic support.

The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance in the United States. The portfolio is listed in the FDA’s 510(k) database.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

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Frequently asked questions

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

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

Which registries list Bioflex, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Bioflex, Inc. include BIOFLEX GARMENTS, ASSORTED MODELS.

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