
N & C Holdings, LLC
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CP Relief Wand Rx - TENS/NMES is an FDA 510(k)-cleared medical device (K252236) manufactured by N & C Holdings, LLC. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 14, 2025. Regulation: 8.

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