Stryker Communications is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stryker Communications - FDA 510(k) Cleared Devices
Recent clearances: VISUM BLADE LED SURGICAL LIGHTING SYSTEM, STRYKER SWITCHPOINT INFINITY 3 CONTROL SYSTEM, MODEL: 067-8001-000
2
Total
2
Cleared
0
Denied
Stryker Communications has 2 FDA 510(k) cleared medical devices. Based in Flower Mound, US.
Historical record: 2 cleared submissions from 2010 to 2013. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Stryker Communications Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Stryker Communications
2 devices