Zephyr Sleep Technologies, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Zephyr Sleep Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: TD Clip
2
Total
2
Cleared
0
Denied
Zephyr Sleep Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Calgary; Alberta, CA.
Historical record: 2 cleared submissions from 2012 to 2019. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Zephyr Sleep Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Zephyr Sleep Technologies, Inc.
2 devices