Entreprise Premont, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Entreprise Premont, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Humask Pro Vision, Humask Pro Vision 3000
1
Total
1
Cleared
0
Denied
Entreprise Premont, Inc. has 1 FDA 510(k) cleared medical devices. Based in Louiseville, CA.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Entreprise Premont, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Enterprise Premont, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Entreprise Premont, Inc.
1 devices