Everyway Medical Instruments Co., Ldt.

FDA Regulatory Profile

Everyway Medical Instruments Co., Ldt. has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 10, 2018

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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) clearances2Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K181849iStim S2 OTC Pain Relief TENSAug 10, 2018
K181207Balego TENS Digital Edition with Accessories for Pain Relief (OTC)Jun 6, 2018