Stimlabs, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stimlabs, LLC - FDA 510(k) Cleared Devices
Recent clearances: Theracor, Corplex P/ Theracor P/ Allacor P, Corplex P / Theracor P / Allacor P
3
Total
3
Cleared
0
Denied
Stimlabs, LLC has 3 FDA 510(k) cleared medical devices. Based in Roswell, US.
Latest FDA clearance: Dec 2025. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stimlabs, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stimlabs, LLC
3 devices