
Lifecore Biomedical, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM is an FDA 510(k)-cleared medical device (K994205) manufactured by Lifecore Biomedical, Inc.. This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 2000. Regulation: 8.