Bostonsight is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bostonsight - FDA 510(k) Cleared Devices
Recent clearances: BostonSight Scleral
2
Total
2
Cleared
0
Denied
Bostonsight has 2 FDA 510(k) cleared medical devices. Based in Needham, US.
Historical record: 2 cleared submissions from 2016 to 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Bostonsight Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Bostonsight
2 devices