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/ Gauss Surgical, Inc.,
Gauss Surgical, Inc.,
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K163507
Triton Sponge System
April 25, 2017
K160338
Triton System
August 5, 2016
K142801
Triton Canister System
March 12, 2015
DEN130015
PIXEL 3 SYSTEM
May 9, 2014
K121274
PIXEL APP
June 27, 2012
K120473
PIXEL APP
April 9, 2012