Balosmark, Inc. is one of 5263 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Balosmark, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Balosmark, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kalamazoo, US.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Balosmark, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Gateway Medical Consulting Services, LLC as regulatory consultant.
Balosmark, Inc. — FDA 510(k) Products and Clearance History
1 devices