Airpharma, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Airpharma, LLC makes
Airpharma, LLC manufactures spacer devices designed to improve the administration of inhaled medications, including the EZ-SPACER and the E-Z SPACER MASK (Small). These products are intended for use with metered-dose inhalers to enhance drug delivery for respiratory conditions.
The company’s portfolio includes devices classified under FDA’s Class I and Class II categories, with regulatory submissions listed via the 510(k) pathway. These products are intended for commercial distribution within the United States.
Catalogue
Ez-Spacer Ref K933090
Regimes: 510(k) Registry: 510(k)E-Z Spacer Mask (Small) Ref K964956
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Airpharma, LLC have in the registry?
The registry currently lists 2 devices for Airpharma, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Airpharma, LLC's devices?
Among its 2 most recently registered devices, Airpharma, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Airpharma, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Airpharma, LLC's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Airpharma, LLC in the registry?
The most recently registered devices listed for Airpharma, LLC include EZ-SPACER and E-Z SPACER MASK (SMALL).