Eicona Corp.
Country not established
- Devices
- 1
What Eicona Corp. makes
Eicona Corp. manufactures the Acupress Vibrator, a Class I medical device designed for therapeutic or relaxation purposes.
The Acupress Vibrator is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Acupress Vibrator Ref K812902
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eicona Corp. have in the registry?
The registry currently lists 1 device for Eicona Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eicona Corp.'s devices?
Among its 1 most recently registered device, Eicona Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Eicona Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eicona Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Eicona Corp. in the registry?
The most recently registered devices listed for Eicona Corp. include ACUPRESS VIBRATOR.