Tri-Gas, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Tri-Gas, Inc. makes
Tri-Gas, Inc. manufactures medical-grade gas mixtures, including blood gas mixtures for respiratory and critical care applications, as well as laser gas mixtures for surgical and dermatological procedures.
The company’s portfolio is regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. Their products are listed in the FDA’s 510(k) database, and the company is based in the United States.
Catalogue
Blood Gas Mixture Ref K932874
Regimes: 510(k) Registry: 510(k)Laser Gas Mixture Ref K935034
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tri-Gas, Inc. have in the registry?
The registry currently lists 2 devices for Tri-Gas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tri-Gas, Inc.'s devices?
Among its 2 most recently registered devices, Tri-Gas, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tri-Gas, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tri-Gas, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tri-Gas, Inc. in the registry?
The most recently registered devices listed for Tri-Gas, Inc. include BLOOD GAS MIXTURE and LASER GAS MIXTURE.