Stellartech Research Corp.
United Statesfrom the FDA registration address FDA establishment FEI 3010653929
- Devices
- 11
- Registrations
- FDA
- FDA recalls
- 0
What Stellartech Research Corp. makes
Stellartech Research Corp. manufactures coagulation systems and radiofrequency generators, including models such as the Stellartech Coagulation System (Models 1100C-115 & 1100C-230), Stellartech 100 Coagulation System, and Stellartech Radiofrequency Generator, Model 1025A-115 and 1025A-230.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Search and filter all 11 devicesCompany details
- FDA FEI number
- 3010653929
- Address
- 560 Cottonwood Dr, Milpitas, CA, 95035
Frequently asked questions
How many devices does Stellartech Research Corp. have in the registry?
The registry currently lists 11 devices for Stellartech Research Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stellartech Research Corp.'s devices?
Among its 11 most recently registered devices, Stellartech Research Corp. has devices listed in FDA 510(k) (11 devices).
What risk classes do Stellartech Research Corp.'s devices fall under?
Among its 11 most recently registered devices, the classes recorded for Stellartech Research Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stellartech Research Corp. in the registry?
The most recently registered devices listed for Stellartech Research Corp. include MODIFICATION TO: STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230), STELLARTECH COAGULATION SYSTEM (MODELS 1100C-115 & 1100C-230), STELLARTECH 100 COAGULATION SYSTEM and STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-115, STELLARTECH RADIOFREQUENCY GENERATOR, MODEL 1025A-230.