Applied Tissue Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Applied Tissue Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: PWD Negative Pressure Wound Therapy System, PWD Platform Wound Dressing 3” x 5” Oblong, Applied Tissue Technologies PWD™ Platform Wound Dressing
3
Total
3
Cleared
0
Denied
Applied Tissue Technologies, LLC has 3 FDA 510(k) cleared medical devices. Based in Hingham, US.
Last cleared in 2022. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Applied Tissue Technologies, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Lakeshore Medical Device Consulting, LLC and Lakeshore Medical Device Consulting.
FDA 510(k) Regulatory Record - Applied Tissue Technologies, LLC
3 devices