ClearanceBrief
Company ยท US

Ki Mobility, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2006 to 2023. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IORWheelchair, Mechanical3
INMChair, With Casters1
ITIWheelchair, Powered1
LBEStroller, Adaptive1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 5, 2023K201869Ki Power Tilt System
Ki Mobility, LLC
ITI
Sep 5, 2023K200583Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTL
Ki Mobility, LLC
IOR
Aug 31, 2023K223533Little Wave Arc; Little Wave Flip
Ki Mobility, LLC
LBE
Aug 31, 2023K223527Little Wave Clik, Rogue XP, Little Wave XP, Spark
Ki Mobility, LLC
IOR
Oct 24, 2006K062660CATALYSY
Ki Mobility, LLC
IOR

Latest recalls

DateFirm and productCodeLinked 510(k)
Nov 19, 2021Ki Mobility Llc
Ki Mobility, Little Wave Tyke (Weight Limit: 95 lbs), Specifically the IFU The Little Wave Tyke is a manually operated device that can be used for medical purposes and is used to assist a disabled pe
Terminated
INMNone listed
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