Union Carbide Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 69
What Union Carbide Corp. makes
Union Carbide Corp. manufactures diagnostic reagents and calibration standards for laboratory use, including enzymatic methods for measuring triglycerides, AST/SGOT, and creatinine, as well as specialized reagents like alizarin sulfonate for analytical testing. Their portfolio also includes portable oxygen reservoir systems and automated immunoassay systems for clinical chemistry, such as the Centria RIA platform and related calibration kits.
The company’s products are regulated under FDA’s 510(k) clearance process, with devices classified as Class I and Class II. These items are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Search and filter all 69 devicesShowing 1-50 of 69
Frequently asked questions
How many devices does Union Carbide Corp. have in the registry?
The registry currently lists 69 devices for Union Carbide Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Union Carbide Corp.'s devices?
Among its 50 most recently registered devices, Union Carbide Corp. has devices listed in FDA 510(k) (50 devices).
What risk classes do Union Carbide Corp.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Union Carbide Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Union Carbide Corp. in the registry?
The most recently registered devices listed for Union Carbide Corp. include CENTRIFICHEM CREATININE, LINDE MARK II OXYGEN RESERV. TYPE OR-4, CENTRIA HPL RIA and CENTRIFICHEM FILTER CALIBRATION SET.