
Lpi, Inc.
Free shipping on orders over $99 · 30-day returns
Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select) is an FDA 510(k)-cleared medical device (K180576) manufactured by Lpi, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 18, 2018. Regulation: 8.