Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL

Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL is an FDA 510(k)-cleared medical device (K200583) manufactured by Ki Mobility, LLC. This device is classified under the Physical Medicine specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 4, 2023. Regulation: 8.