Sublimed is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Sublimed - FDA 510(k) Cleared Devices
Recent clearances: actiTENS mini, actiTENS
2
Total
2
Cleared
0
Denied
Sublimed has 2 FDA 510(k) cleared medical devices. Based in Moirans, FR.
Latest FDA clearance: Jan 2026. Active since 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Sublimed Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Medical Device Academy, Inc. and Medical Device Academy.
FDA 510(k) Regulatory Record - Sublimed
2 devices