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Bostonsight

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K183175BostonSight ScleralJanuary 4, 2019
K161461BostonSight PD Prosthetic DeviceJuly 25, 2016