Tepha, Inc. - FDA 510(k) Cleared Devices
18
Total
17
Cleared
1
Denied
Tepha, Inc. has 17 FDA 510(k) cleared general & plastic surgery devices. Based in Cambridge, US.
Latest FDA clearance: Apr 2024. Active since 2007.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Tepha, Inc.
18 devices
Cleared
Apr 09, 2024
GalaFLEX LITE Scaffold
General & Plastic Surgery
113d
Cleared
Aug 19, 2021
SurgiLattice scaffold
General & Plastic Surgery
359d
Cleared
May 27, 2021
GalaSTITCH Absorbable Monofilament Suture
General & Plastic Surgery
28d
Cleared
Feb 23, 2017
GalaFORM 3D
General & Plastic Surgery
128d
Cleared
Aug 23, 2016
GalaSHAPE 3D
General & Plastic Surgery
127d
Cleared
May 21, 2014
GALAFLEX MESH
General & Plastic Surgery
78d
Cleared
Sep 05, 2013
TEPHAFLEX BRAIDED SUTURE
General & Plastic Surgery
38d
Cleared
May 07, 2013
TEPHAFLEX MELTBLOWN CONSTRUCT
General & Plastic Surgery
88d
Cleared
Feb 15, 2012
TEPHAFLEX LIGHT MESH
General & Plastic Surgery
58d
Cleared
Feb 15, 2012
TEPHAFLEX MESH
General & Plastic Surgery
58d
Cleared
Sep 26, 2011
TEPHAFLEX MESH
General & Plastic Surgery
80d
Cleared
Aug 30, 2010
TEPHAFLEX COMPOSITE MESH
General & Plastic Surgery
115d