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Spirox, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K161191
Latera Absorbable Nasal Implant
June 23, 2016
K152958
INEX Absorbable Nasal Implant
December 4, 2015
K132920
SPIROX INEX DEVICE
June 10, 2014