Inmed Ltda.
Country not established
- Devices
- 3
What Inmed Ltda. makes
Inmed Ltda. manufactures conductive gels and electrodes for electrodiagnostic procedures, including the LEKTROGEL (Model LK3001) for skin preparation and signal transmission, as well as the CSF400 and CSF600 for specific electrophysiological applications. The ULTRAEKOGEL (Models EK 2000 & EK 2001) is designed for use in electromyography and nerve conduction studies, enhancing electrode adhesion and signal quality.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. The portfolio is listed in the FDA’s 510(k) database, reflecting compliance with U.S. medical device authorisation requirements. Inmed Ltda. operates from the United States.
Catalogue
Lektrogel, Model LK3001 Ref K030887
Regimes: 510(k) Registry: 510(k)CSF400 And CSF600 Ref K030081
Regimes: 510(k) Registry: 510(k)Ultraekogel Models Ek 2000 & Ek 2001 Ref K030889
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Inmed Ltda. have in the registry?
The registry currently lists 3 devices for Inmed Ltda.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inmed Ltda.'s devices?
Among its 3 most recently registered devices, Inmed Ltda. has devices listed in FDA 510(k) (3 devices).
What risk classes do Inmed Ltda.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Inmed Ltda.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Inmed Ltda. in the registry?
The most recently registered devices listed for Inmed Ltda. include LEKTROGEL, MODEL LK3001, CSF400 AND CSF600 and ULTRAEKOGEL MODELS EK 2000 & EK 2001.