Oximetrix, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 12
What Oximetrix, Inc. makes
Oximetrix, Inc. manufactures medical devices for monitoring and managing blood flow, oxygenation, and thermal regulation in clinical settings. Their portfolio includes heparin-coated and flow-directed catheters for thermal dilution measurements, in vivo oximeters for real-time oxygen saturation monitoring, and infusion pumps for wearable fluid administration. Additional products include hemostatic surgical systems, optical catheters with computer integration, and systems for cardiopulmonary bypass (CPB) oxygen saturation monitoring.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory clearance obtained through the 510(k) pathway. These products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. Oximetrix, Inc. is headquartered in the United States.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Oximetrix, Inc. have in the registry?
The registry currently lists 12 devices for Oximetrix, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oximetrix, Inc.'s devices?
Among its 12 most recently registered devices, Oximetrix, Inc. has devices listed in FDA 510(k) (12 devices).
What risk classes do Oximetrix, Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Oximetrix, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oximetrix, Inc. in the registry?
The most recently registered devices listed for Oximetrix, Inc. include OPTICATH HEPARIN COATED, FLOW-DIRECT, CATHETER, THERMAL DILUTION FIBEROPTIC, HEMO STATIC/ESU SCALPEL SYSTEM and OPTICATH.