OrthoGrid Systems, Inc.

FDA Regulatory Profile

OrthoGrid Systems, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 29, 2026.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260077OrthoGrid Hip AI® 4.0May 29, 2026
K210136PhantomMSK HipFebruary 18, 2021
K192279PhantomMSK TraumaDecember 7, 2019
K182332PhantomMSKFebruary 15, 2019