SubNovii Advanced Plasma Technology— 510(k) K201738

Name: FDA 510(k) clearance K201738
Creator: U.S. Food and Drug Administration
Published: 2020-09-10

Substantially Equivalent

Cartessa Aesthetics

FDA 510(k) clearance K201738 for SubNovii Advanced Plasma Technology, Substantially Equivalent on 2020-09-10. Applicant: Cartessa Aesthetics. Device class: 2.

Clearance details

Applicant: Cartessa Aesthetics
Product code: Code GEI
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2020-06-25
Decision date: 2020-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GEI

view all

K254185 — Potenza Prime2026-09-11
K262364 — Ellian Enigma RF Device2026-09-02
K253859 — Scarlet Pro (Scarlet Pro)2026-08-27
K252535 — Inno-Switch Laparoscopic Instruments2026-08-25
K261179 — AlphaTriPart - Monopolar MIC Instruments2026-07-22

Adverse events under product code GEI

product code GEI

Death: 133
Injury: 7,585
Malfunction: 35,808
Other: 44
Total: 43,570

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.