Dermadry Laboratories, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Dermadry Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Dermadry
1
Total
1
Cleared
0
Denied
Dermadry Laboratories, Inc. has 1 FDA 510(k) cleared medical devices. Based in Montreal, CA.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Dermadry Laboratories, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lok North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Dermadry Laboratories, Inc.
1 devices