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Radiation Products Design, Inc.

Country not established FDA establishment FEI 2182762

Devices
8
Registrations
FDA
FDA recalls
0

What Radiation Products Design, Inc. makes

Radiation Products Design, Inc. manufactures specialized medical devices for radiation therapy and patient positioning, including adjustable treatment chairs, head and face holders, bite block systems, and back supports with arm positioners. Their product line also includes table inserts like Mylar and tennis racket designs, as well as precision tools such as point-to-point leveling devices for treatment setup.

All listed devices fall under Class II regulatory classification in the U.S. and are authorized via 510(k) clearance through the FDA. The company operates from the United States and maintains its products in the FDA’s 510(k) registry.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

Company details

FDA FEI number
2182762
Address
5218 Barthel Industrial Dr Ne, ALBERTVILLE, MN, 55301

Frequently asked questions

How many devices does RADIATION PRODUCTS DESIGN, INC. have in the registry?

The registry currently lists 8 devices for RADIATION PRODUCTS DESIGN, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list RADIATION PRODUCTS DESIGN, INC.'s devices?

Among its 8 most recently registered devices, RADIATION PRODUCTS DESIGN, INC. has devices listed in FDA 510(k) (8 devices).

What risk classes do RADIATION PRODUCTS DESIGN, INC.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for RADIATION PRODUCTS DESIGN, INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from RADIATION PRODUCTS DESIGN, INC. in the registry?

The most recently registered devices listed for RADIATION PRODUCTS DESIGN, INC. include MYVACET 5-07, 7-00 AND 9-40, ADJUSTABLE HEAD & FACE HOLDER, BITE BLOCK SYSTEM and ELEV. BACK SUPPORT W/ADJ. ARM POSITIONER.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.