Tissue Regeneration Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tissue Regeneration Technologies - FDA 510(k) Cleared Devices
Recent clearances: OrthoGold, OrthoGold 100
2
Total
2
Cleared
0
Denied
Tissue Regeneration Technologies has 2 FDA 510(k) cleared medical devices. Based in Woodstock, US.
Historical record: 2 cleared submissions from 2018 to 2019. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Tissue Regeneration Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Tissue Regeneration Technologies
2 devices