Company ยท US
Gauss Surgical, Inc.,
FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2017. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Apr 25, 2017 | K163507 | Triton Sponge System Gauss Surgical, Inc., | PBZ |
| Aug 5, 2016 | K160338 | Triton System Gauss Surgical, Inc., | PBZ |
| Mar 12, 2015 | K142801 | Triton Canister System Gauss Surgical, Inc., | PBZ |
| May 9, 2014 | DEN130015 | PIXEL 3 SYSTEM Gauss Surgical, Inc., | PBZ |
| Jun 27, 2012 | K121274 | PIXEL APP Gauss Surgical, Inc., | LWH |
| Apr 9, 2012 | K120473 | PIXEL APP Gauss Surgical, Inc., | LWH |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||