
Karlin Technology, Inc.
Free shipping on orders over $99 · 30-day returns
SPINAL NEEDLE is an FDA 510(k)-cleared medical device (K882073) manufactured by Karlin Technology, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on July 17, 1988. Regulation: 8.