Entellus Medical, Inc. (Aka Stryker Ent) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Entellus Medical, Inc. (Aka Stryker Ent) - FDA 510(k) Cleared Devices
Recent clearances: LATERA Absorbable Nasal Implant System
1
Total
1
Cleared
0
Denied
Entellus Medical, Inc. (Aka Stryker Ent) has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Entellus Medical, Inc. (Aka Stryker Ent) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Entellus Medical, Inc. (Aka Stryker Ent)
1 devices