
Jeil Medical Corporation
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J TAC MODEL JT-MD-035, JT-MD-040, JT-MD-045, JT-CL-030 is an FDA 510(k)-cleared medical device (K101902) manufactured by Jeil Medical Corporation. 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 7, 2011. Regulation: 8.