Aeiomed, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Aeiomed, Inc. makes
Aeiomed, Inc. makes CPAP systems and related patient interfaces, including the AURA CPAP System, Model 300157 CPAP System, and reusable headrests with nasal seals designed for use with CPAP therapy.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Aura Cpap System Ref K042945
Regimes: 510(k) Registry: 510(k)Reusable Headrest With Nasal Seal Ref K072993
Regimes: 510(k) Registry: 510(k)Aura Cpap Patient Interface Ref K042130
Regimes: 510(k) Registry: 510(k)Model 300157 Cpap System Ref K100121
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aeiomed, Inc. have in the registry?
The registry currently lists 4 devices for Aeiomed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aeiomed, Inc.'s devices?
Among its 4 most recently registered devices, Aeiomed, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Aeiomed, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Aeiomed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aeiomed, Inc. in the registry?
The most recently registered devices listed for Aeiomed, Inc. include AURA CPAP SYSTEM, REUSABLE HEADREST WITH NASAL SEAL, AURA CPAP PATIENT INTERFACE and MODEL 300157 CPAP SYSTEM.