Snyder Industries, Inc. is one of 18397 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Snyder Industries, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Med-Tainer Single Deposit Container
1
Total
1
Cleared
0
Denied
Snyder Industries, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lincoln, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Snyder Industries, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Snyder Industries, Inc.
1 devices