Optovent AB
Country not established
- Devices
- 2
What Optovent AB makes
Optovent AB manufactures respiratory support devices, including the OptoVent RESPONS and OptoVent RENEE (a variant without a pulse oximetry module). These devices are designed for non-invasive ventilation, providing controlled ventilation and monitoring for patients requiring respiratory assistance.
The company’s products fall under FDA Class II devices and are listed via the 510(k) pathway in the United States. Optovent AB is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Optovent AB have in the registry?
The registry currently lists 2 devices for Optovent AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Optovent AB's devices?
Among its 2 most recently registered devices, Optovent AB has devices listed in FDA 510(k) (2 devices).
What risk classes do Optovent AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Optovent AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Optovent AB in the registry?
The most recently registered devices listed for Optovent AB include OPTOVENT RESPIRATORY MONITOR MODEL NUMBER RR 9700 and OPTOVENT RESPONS, OPTOVENT RENEE (OPTOVENT RESPONS WITHOUT PULSE OXIMETRY MODULE).