Medical Device Manufacturer · US , Bedford , MA

Cynosure, Inc. - FDA 510(k) Cleared Devices

98 submissions · 98 cleared · Since 1992
98
Total
98
Cleared
0
Denied

Cynosure, Inc. has 98 FDA 510(k) cleared general & plastic surgery devices. Based in Bedford, US.

Historical record: 98 cleared submissions from 1992 to 2019.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Cynosure, Inc.

98 devices
1-12 of 98

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