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Akros Medical

FDA Regulatory Profile

Akros Medical has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 6, 2020

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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) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K200361Akros Scruture Anchor LisFranc Repair KitApr 6, 2020
K173550Akros FibuLink™ Syndesmosis Repair KitDec 14, 2017
K162805Akros Fibulink Syndesmosis Repair KitJan 10, 2017

FDA data resources