Gemini, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Gemini, Inc. makes
Gemini, Inc. manufactures medical devices including the GEMENI QUICK-MB SEPARATION KIT and the GEMENI CK-MB ISOENZYME ABNORMAL SERUM, which are diagnostic test kits used for laboratory testing.
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Gemini, Inc. is based in the US.
Catalogue
Gemeni Quick-Mb Separation Kit Ref K810534
Regimes: 510(k) Registry: 510(k)Gemeni Ck-Mb Isoenzyme Abnormal Serum Ref K810870
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gemini, Inc. have in the registry?
The registry currently lists 2 devices for Gemini, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gemini, Inc.'s devices?
Among its 2 most recently registered devices, Gemini, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gemini, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gemini, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gemini, Inc. in the registry?
The most recently registered devices listed for Gemini, Inc. include GEMENI QUICK-MB SEPARATION KIT and GEMENI CK-MB ISOENZYME ABNORMAL SERUM.