TELA Bio, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Liora Monofilament Scaffold, OviTex PRS (Long-Term Resorbable), OviTex PRS
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - TELA Bio, Inc. General & Plastic Surgery ✕
4 devices
Cleared
Sep 28, 2026
Liora Monofilament Scaffold
General & Plastic Surgery
228d
Cleared
Dec 19, 2024
OviTex PRS (Long-Term Resorbable)
General & Plastic Surgery
29d
Cleared
May 22, 2024
OviTex PRS
General & Plastic Surgery
29d
Cleared
Dec 11, 2014
OVINE TISSUE MATRIX(OTM)
General & Plastic Surgery
231d