Precifit Medical, Ltd.

FDA Regulatory Profile

Precifit Medical, Ltd. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jun 8, 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) clearances4Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K173189Lumfuse TPJun 8, 2018
K172568CervageMay 4, 2018
K171630LumFuse-TPJul 25, 2017
K163327Precifit Medical Kirschner WiresMay 8, 2017