Qmenta Care Platform Family

Qmenta Care Platform Family is an FDA 510(k)-cleared medical device (K202718) manufactured by Mint Labs, Inc., D/B/A. Qmenta. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 15, 2021. Regulation: 8.