Radius Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Radius Intl., Inc. makes
Radius Intl., Inc. manufactures enteral feeding tubes, manual wheelchair models (including Cobra, Viper, Swing, Olympia, and Mobil variants), and gastrostomy-related products. These include low-profile gastrostomy tube kits, percutaneous endoscopic gastrostomy (PEG) pull and push-over-the-guide-wire kits, and associated accessories for nutritional support and patient mobility.
The company’s devices are classified under FDA’s Class I and Class II categories, with relevant products listed via the 510(k) pathway. These products are regulated under US medical device laws, and the company operates from the United States.
Catalogue
Radius Enteral Feeding Tube Ref K930510
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Radius Low Profile Gastrostomy Tube Kit Ref K971901
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Radius Intl., Inc. have in the registry?
The registry currently lists 5 devices for Radius Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Radius Intl., Inc.'s devices?
Among its 5 most recently registered devices, Radius Intl., Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Radius Intl., Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Radius Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Radius Intl., Inc. in the registry?
The most recently registered devices listed for Radius Intl., Inc. include RADIUS ENTERAL FEEDING TUBE, RADIUS MANUAL WHWWLCHAIRS (COBRA, VIPER, SWING, OLYMPIA, AND MOBIL MODELS), RADIUS LOW PROFILE GASTROSTOMY TUBE KIT and RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT.