Chromogenex Technologies, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 3
What Chromogenex Technologies, Ltd. makes
Chromogenex Technologies, Ltd. manufactures the I-LIPO, a medical device available in two voltage models (A00-1238 for 230V and A00-1239 for 120V). This device is designed for liposuction procedures, assisting in fat removal through controlled aspiration.
The I-LIPO is classified as a Class II medical device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Chromolite Ep Ref K081619
Regimes: 510(k) Registry: 510(k)I-Lipo System Ref K111501
Regimes: 510(k) Registry: 510(k)I-Lipo, Models A00-1238 (230V), A00-1239 (120V) Ref K101366
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chromogenex Technologies, Ltd. have in the registry?
The registry currently lists 3 devices for Chromogenex Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chromogenex Technologies, Ltd.'s devices?
Among its 3 most recently registered devices, Chromogenex Technologies, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Chromogenex Technologies, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Chromogenex Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chromogenex Technologies, Ltd. in the registry?
The most recently registered devices listed for Chromogenex Technologies, Ltd. include CHROMOLITE EP, I-LIPO SYSTEM and I-LIPO, MODELS A00-1238 (230V), A00-1239 (120V).