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Axis Orthopaedics

FDA Regulatory Profile

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

Latest 510(k)
Nov 16, 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) clearances3Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K181140Axis Chena Cervical PEEK Spacer SystemNov 16, 2018
K180301AXIS 5.5 Lumbar Pedicle Screw SystemApr 10, 2018
K173867Axis Anterior Cervical Plate SystemApr 5, 2018

FDA data resources