Oeco
Country not established
- Devices
- 2
What Oeco makes
Oeco manufactures medical devices including nasal cannulas for oxygen delivery and apnea monitors designed to track respiratory events during sleep. These products are intended for use in clinical and home settings to support patient oxygenation and respiratory assessment.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with several products listed via the 510(k) clearance pathway. These devices are based in the United States and comply with applicable U.S. regulatory standards.
Catalogue
Oeco Nasal Cannula Ref K811789
Regimes: 510(k) Registry: 510(k)Oeco Apnea Monitor Ref K811628
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oeco have in the registry?
The registry currently lists 2 devices for Oeco. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oeco's devices?
Among its 2 most recently registered devices, Oeco has devices listed in FDA 510(k) (2 devices).
What risk classes do Oeco's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Oeco's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oeco in the registry?
The most recently registered devices listed for Oeco include OECO NASAL CANNULA and OECO APNEA MONITOR.