Reflexonic, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Reflexonic, LLC makes
Reflexonic, LLC manufactures penile vibratory stimulation devices designed for medical use, including the Viberect Penile Vibratory Stimulation Device. These devices are intended to assist with sexual health interventions and may be used in clinical or therapeutic settings.
The company’s portfolio is regulated under Class II medical devices in the United States, with devices authorised through the FDA’s 510(k) clearance process. The manufacturer is based in the US.
Catalogue
Viberect Penile Vibratory Stimulation Device Ref K142304
Regimes: 510(k) Registry: 510(k)Viberect Penile Vibratory Stimulation Device Ref K110566
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Reflexonic, LLC have in the registry?
The registry currently lists 2 devices for Reflexonic, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Reflexonic, LLC's devices?
Among its 2 most recently registered devices, Reflexonic, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Reflexonic, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Reflexonic, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Reflexonic, LLC in the registry?
The most recently registered devices listed for Reflexonic, LLC include Viberect Penile Vibratory Stimulation Device.