Inspiron Corp.
United StatesFDA applicant, unverified
- Devices
- 20
What Inspiron Corp. makes
Inspiron Corp. manufactures respiratory and anesthesia equipment, including oxygen concentrators, liquid oxygen systems, nasal cannulas, and anesthesia circuits. Their product line also features ventilation setups, nebulizers, bacterial filters, humidifiers, and inspiratory/expiratory muscle exercisers, alongside intravenous preparation kits.
The company is based in the United States and maintains a portfolio of Class I and Class II medical devices. These products are listed within the FDA 510(k) regulatory registry.
Catalogue
Search and filter all 20 devicesFrequently asked questions
How many devices does Inspiron Corp. have in the registry?
The registry currently lists 20 devices for Inspiron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inspiron Corp.'s devices?
Among its 20 most recently registered devices, Inspiron Corp. has devices listed in FDA 510(k) (20 devices).
What risk classes do Inspiron Corp.'s devices fall under?
Among its 20 most recently registered devices, the classes recorded for Inspiron Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inspiron Corp. in the registry?
The most recently registered devices listed for Inspiron Corp. include MANIFOLD & NEBU. FOR SINGLE LINE MACH., PEDIATRIC ANESTHESIA CIRCUIT, FILTER, BACTERIA (#2290) and INSPIRON LIQUID OXYGEN SYSTEM.