Gauss Surgical, Inc., - FDA 510(k) Cleared Devices
6
Total
5
Cleared
1
Denied
Gauss Surgical, Inc., has 5 FDA 510(k) cleared medical devices. Based in Cupertino, US.
Historical record: 5 cleared submissions from 2012 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Gauss Surgical, Inc., Filter by specialty or product code using the sidebar.
6 devices
Cleared
Apr 25, 2017
Triton Sponge System
General & Plastic Surgery
132d
Cleared
Aug 05, 2016
Triton System
General & Plastic Surgery
179d
Cleared
Mar 12, 2015
Triton Canister System
General & Plastic Surgery
164d
Not Cleared
May 09, 2014
PIXEL 3 SYSTEM
General & Plastic Surgery
459d
Cleared
Jun 27, 2012
PIXEL APP
General & Plastic Surgery
61d
Cleared
Apr 09, 2012
PIXEL APP
General & Plastic Surgery
53d