Mesynthe, Ltd. is one of 5203 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mesynthe, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Mesynthe, Ltd. has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mesynthe, Ltd. Filter by specialty or product code using the sidebar.
Mesynthe, Ltd. — FDA 510(k) Products and Clearance History
1 devices