Medical Device Manufacturer · US , Plymouth , MN

Stryker Ent - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2020
3
Total
3
Cleared
0
Denied

Stryker Ent has 3 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Historical record: 3 cleared submissions from 2020 to 2020. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Stryker Ent Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Stryker Ent

3 devices
1-3 of 3
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All3 Ear, Nose, Throat 3