
Stryker Corp.
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STRYKERSCOPE TM/ORTHOSCOPE TM/STRYKER MINISCOPE TM is an FDA 510(k)-cleared medical device (K871816) manufactured by Stryker Corp.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 2, 1987. Regulation: 8.