Clonetics Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Clonetics Corp. makes
Clonetics Corp. produces cell culture media and growth supplements, including specialized formulations like Melanocyte Growth Medium (MGM), Keratinocyte Growth Medium (KGM), and Endothelial Growth Medium (EGM), designed for in vitro cell expansion. The company also offers the EPIPACK, a kit for epithelial cell culture applications.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Epipack Ref K880999
Regimes: 510(k) Registry: 510(k)Melanocyte Growth Medium (Mgm) Ref K890700
Regimes: 510(k) Registry: 510(k)Keratinocyte Growth Medium (Kgm) Ref K881000
Regimes: 510(k) Registry: 510(k)Endothelial Growth Medium (Egm) Ref K890701
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clonetics Corp. have in the registry?
The registry currently lists 4 devices for Clonetics Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clonetics Corp.'s devices?
Among its 4 most recently registered devices, Clonetics Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Clonetics Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Clonetics Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Clonetics Corp. in the registry?
The most recently registered devices listed for Clonetics Corp. include EPIPACK, MELANOCYTE GROWTH MEDIUM (MGM), KERATINOCYTE GROWTH MEDIUM (KGM) and ENDOTHELIAL GROWTH MEDIUM (EGM).