Neo-Tech, Inc.
Country not established
- Devices
- 1
What Neo-Tech, Inc. makes
Neo-Tech, Inc. manufactures the HOLDE.T. Endotracheal Tube Stabilization Bar, a device designed to secure endotracheal tubes in place during medical procedures.
The company’s portfolio is regulated under FDA’s Class I device classification and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Holde.t. Endotracheal Tube Stabilization Bar Ref K934288
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neo-Tech, Inc. have in the registry?
The registry currently lists 1 device for Neo-Tech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neo-Tech, Inc.'s devices?
Among its 1 most recently registered device, Neo-Tech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neo-Tech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neo-Tech, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Neo-Tech, Inc. in the registry?
The most recently registered devices listed for Neo-Tech, Inc. include HOLDE.T. ENDOTRACHEAL TUBE STABILIZATION BAR.