FDA.reportPublic FDA data

Ki Mobility

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30059053213005905321Ki Mobility1Y2026-01-015201 WOODWARD DR Stevens Point WI US 54481

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
790522037833548K240267Klaxon (Twist); Klaxon (Twist R)ITI2025-01-10
790521283953744K223533Little Wave Arc; Little Wave FlipLBE2023-08-31
790521981509154K223527Little Wave Clik, Rogue XP, Little Wave XP, SparkIOR2023-08-31
790521309992682K201869Ki Power Tilt SystemITI2023-09-05
790521442289547K200583Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTLIOR2023-09-05
790521691506651K062660CATALYSYIOR2006-10-24
790521884606839
790521098044766
790521199801131
790521391091090
790521604699279
790521674087405

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
IOR32023-09-05
ITI22025-01-10
LBE12023-08-31