Cryos Technologies, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Cryos Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CryoVizion System
1
Total
1
Cleared
0
Denied
Cryos Technologies, Inc. has 1 FDA 510(k) cleared medical devices. Based in Joliette, CA.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Cryos Technologies, 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 - Cryos Technologies, Inc.
1 devices