Currently Under FDA Review
LiviWell is developing innovative solutions for women's health.
Our first medical device is currently being evaluated by the U.S. Food and Drug Administration
under the 510(k) review process.
Clearance timing subject to FDA review.
Pending FDA clearance. Not available for sale in the United States.
For inquiries, please contact:
info@liviwell.com
info@liviwell.com