Stronghold Group, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stronghold Group, LLC - FDA 510(k) Cleared Devices
Recent clearances: Stronghold Group Nitrile Examination Glove, Powder Free
1
Total
1
Cleared
0
Denied
Stronghold Group, LLC has 1 FDA 510(k) cleared medical devices. Based in Lewisberry, US.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Stronghold Group, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Stronghold Group, LLC
1 devices