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Freerider Corporation

FDA Regulatory Profile

Freerider Corporation has 0 FDA recalls, 3 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jan 14, 2026 · NAI
Latest 510(k)
Mar 20, 2017

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections3Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 14, 2026Kaohsiung City, TaiwanDevicesNo Action Indicated (NAI)3003820676
Sep 21, 2017Kaohsiung City, TaiwanDevicesVoluntary Action Indicated (VAI)3003820676
Mar 19, 2014Kaohsiung City, TaiwanDevicesNo Action Indicated (NAI)3003820676

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K160139Luggie ChairMar 20, 2017
K151944Luggie SuperSep 10, 2015
K133187FREERIDER FR1, models FR1-13, FR1-15, FR1-17Jan 8, 2015
K033370POWERED WHEELCHAIR, MODEL FR168WNov 28, 2003

FDA data resources