Orthosoft Inc. (d/b/a) Zimmer CAS

FDA Regulatory Profile

Orthosoft Inc. (d/b/a) Zimmer CAS appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 4, 2026.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Known Names

orthosoft, inc. dba zimmer cas, orthosoft inc. (d/b/a) zimmer cas), orthosoft inc (d/b/a zimmer cas), orthosoft inc. (d/b/a) zimmer cas

Recent 510(k) Clearances

K-NumberDeviceDate
K261510Signature™ ONE SystemJune 4, 2026
K260582ROSA® Shoulder SystemMay 21, 2026
K260104Signature™ ONE SystemFebruary 4, 2026
K251314Rosa® Knee SystemNovember 13, 2025
K242864ROSA® Knee SystemOctober 18, 2024