
Smith & Nephew, Inc.
Free shipping on orders over $99 · 30-day returns
SMITH & NEPHEW DAYLIGHTER(TM) is an FDA 510(k)-cleared medical device (K873786) manufactured by Smith & Nephew, 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 October 22, 1987. Regulation: 8.