Autogenesis, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Autogenesis, Inc. makes
Autogenesis, Inc. manufactures automated cell processing systems, including the AUTOGENESIS AUTOMATOR 2000 (Model SC2000) and AUTOGENESIS AUTOMATOR (Model M1000), designed for controlled cell culture and expansion in laboratory settings.
These devices are classified as Class II under FDA regulations and are recorded in the 510(k) clearance database. The company is based in the United States.
Catalogue
Autogenesis Automator 2000 Model Number SC2000 Ref K981423
Regimes: 510(k) Registry: 510(k)Autogenesis Automator, Model M1000 Ref K013818
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Autogenesis, Inc. have in the registry?
The registry currently lists 2 devices for Autogenesis, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Autogenesis, Inc.'s devices?
Among its 2 most recently registered devices, Autogenesis, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Autogenesis, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Autogenesis, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Autogenesis, Inc. in the registry?
The most recently registered devices listed for Autogenesis, Inc. include AUTOGENESIS AUTOMATOR 2000 MODEL NUMBER SC2000 and AUTOGENESIS AUTOMATOR, MODEL M1000.