
Deringer-Ney, Inc.
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GDC 802-DEVELOPMENT NAME is an FDA 510(k)-cleared medical device (K792210) manufactured by Deringer-Ney, 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 November 19, 1979. Regulation: 8.