Intertex Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Intertex Medical, Inc. makes
Intertex Medical, Inc. manufactures the NEO-LINK, a disposable neonatal airway connector designed for use in infant respiratory support systems.
The NEO-LINK is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Trachestomy & Nasal Suctioning Kit #- Ref K830711
Regimes: 510(k) Registry: 510(k)Neo-Link, Disposable Neonatal Air Way Connector Ref K952824
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intertex Medical, Inc. have in the registry?
The registry currently lists 2 devices for Intertex Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intertex Medical, Inc.'s devices?
Among its 2 most recently registered devices, Intertex Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Intertex Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Intertex Medical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Intertex Medical, Inc. in the registry?
The most recently registered devices listed for Intertex Medical, Inc. include TRACHESTOMY & NASAL SUCTIONING KIT #- and NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTOR.