Smith & Nephew, Inc.
MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI)
SKU K864307UPC EIC
In Stock
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IFDA 510(k) Cleared (K864307)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew, Inc.
Free shipping on orders over $99 · 30-day returns
MAX-I-PROBE PERIDONTAL/ENDODONTIC PROBE(TM) (MODI) is an FDA 510(k)-cleared medical device (K864307) manufactured by Smith & Nephew, Inc.. This device is classified under the Dental specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 17, 1986. Regulation: 8.
