Intavent Intl. S.A.
Country not established
- Devices
- 1
What Intavent Intl. S.A. makes
Intavent International S.A. manufactures the Intavent Laryngeal Mask, a reusable airway management device designed for use in surgical and emergency procedures to maintain an open airway during anesthesia or resuscitation.
The company’s product portfolio is regulated under Class I medical devices in the United States, with the Intavent Laryngeal Mask authorised via the FDA’s 510(k) clearance process. The company is based in the US.
Catalogue
Intavent Laryngeal Mask Ref K904834
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intavent Intl. S.A. have in the registry?
The registry currently lists 1 device for Intavent Intl. S.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intavent Intl. S.A.'s devices?
Among its 1 most recently registered device, Intavent Intl. S.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Intavent Intl. S.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Intavent Intl. S.A.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Intavent Intl. S.A. in the registry?
The most recently registered devices listed for Intavent Intl. S.A. include INTAVENT LARYNGEAL MASK.