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/ Osteomni, Inc.
Osteomni, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K260850
OSTEOMNI SPINAL CAGES SYSTEM
May 12, 2026
K254247
OSTEOMNI SPINAL FIXATION SYSTEM
February 24, 2026