Spirox, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K161191Latera Absorbable Nasal ImplantJune 23, 2016
K152958INEX Absorbable Nasal ImplantDecember 4, 2015
K132920SPIROX INEX DEVICEJune 10, 2014