Medisonic U.S.A., Inc.
Country not established
- Devices
- 5
What Medisonic U.S.A., Inc. makes
Medisonic U.S.A., Inc. manufactures respiratory therapy devices, including ultrasonic and standard inhalers, oxygen flow controllers, and nebulizers designed for medical use. Their products are intended for delivering medications via inhalation and managing oxygen delivery in clinical settings.
The company’s portfolio consists of Class II medical devices, each authorised through the FDA’s 510(k) clearance process. These devices are listed under U.S. regulatory requirements and are based in the United States.
Catalogue
Medisonic Humdifier/Inhaler Ref K901114
Regimes: 510(k) Registry: 510(k)Medivac Ref K924577
Regimes: 510(k) Registry: 510(k)Medisonic Ultra-Sonic Inhaler Ref K894961
Regimes: 510(k) Registry: 510(k)Medisonic Oxygen Flow Controller Ref K923660
Regimes: 510(k) Registry: 510(k)Medisonic Pneu-Neb Ref K896192
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medisonic U.S.A., Inc. have in the registry?
The registry currently lists 5 devices for Medisonic U.S.A., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medisonic U.S.A., Inc.'s devices?
Among its 5 most recently registered devices, Medisonic U.S.A., Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Medisonic U.S.A., Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Medisonic U.S.A., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medisonic U.S.A., Inc. in the registry?
The most recently registered devices listed for Medisonic U.S.A., Inc. include MEDISONIC HUMDIFIER/INHALER, MEDIVAC, MEDISONIC ULTRA-SONIC INHALER and MEDISONIC OXYGEN FLOW CONTROLLER.