Medical Device Manufacturer · US , Cambridge , MA

Tepha, Inc.

18 submissions · 17 cleared · Since 2007
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.

18 devices
1–12 of 18
GalaFLEX LITE Scaffold
K233999 · OOD Surgical Film · General & Plastic Surgery
Apr 2024 113d
SurgiLattice scaffold
K202425 · OOD Surgical Film · General & Plastic Surgery
Aug 2021 359d
GalaSTITCH Absorbable Monofilament Suture
K211307 · NWJ Suture, Recombinant Technology · General & Plastic Surgery
May 2021 28d
GalaFORM 3D
K162922 · OOD Surgical Film · General & Plastic Surgery
Feb 2017 128d
GalaSHAPE 3D
K161092 · OOD Surgical Film · General & Plastic Surgery
Aug 2016 127d
GALAFLEX MESH
K140533 · OOD Surgical Film · General & Plastic Surgery
May 2014 78d
TEPHAFLEX BRAIDED SUTURE
K132348 · NWJ Suture, Recombinant Technology · General & Plastic Surgery
Sep 2013 38d
TEPHAFLEX MELTBLOWN CONSTRUCT
K130326 · OOD Surgical Film · General & Plastic Surgery
May 2013 88d
TEPHAFLEX LIGHT MESH
K113721 · OOD Surgical Film · General & Plastic Surgery
Feb 2012 58d
TEPHAFLEX MESH
K113723 · OOD Surgical Film · General & Plastic Surgery
Feb 2012 58d
TEPHAFLEX MESH
K111946 · OOD Surgical Film · General & Plastic Surgery
Sep 2011 80d
TEPHAFLEX COMPOSITE MESH
K101287 · OWT Mesh, Surgical, Absorbable, Abdominal Hernia · General & Plastic Surgery
Aug 2010 115d
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