Hemogenetics, Inc.
Country not established
- Devices
- 1
What Hemogenetics, Inc. makes
Hemogenetics, Inc. manufactures diagnostic devices used for blood typing and compatibility testing, including light-based test systems for identifying blood group antigens. These tools assist in ensuring accurate blood type determination for transfusion compatibility assessments.
The company’s portfolio is regulated under Class II medical devices in the United States, with devices authorised through the FDA’s 510(k) clearance process. Products are listed in the FDA’s 510(k) database, reflecting compliance with US regulatory requirements.
Catalogue
Light Test Ref K834598
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hemogenetics, Inc. have in the registry?
The registry currently lists 1 device for Hemogenetics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hemogenetics, Inc.'s devices?
Among its 1 most recently registered device, Hemogenetics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Hemogenetics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hemogenetics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hemogenetics, Inc. in the registry?
The most recently registered devices listed for Hemogenetics, Inc. include LIGHT TEST.