Bovie Icon Vs General Purpose Rf Generator, Model: VS300

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K092383 ↗

FDA Product Code

GEI

Device Class

Class II

Regulation

21 CFR Part 878.4400

Advisory Committee

General, Plastic Surgery

FDA Decision

SESE Substantially Equivalent

• Bovie Resistick II Coated Electrosurgical Electrodes

  Class II

  FDA 510(k) K093025 Active Cleared 22 Dec 2009

• Cautery; Low Temperature (Fineadjustable Fine Tip, Elongated Fine Tip, Micro Fine Tip)

  Class II

  FDA 510(k) K121441 Active Cleared 20 Jul 2012

• Renuvion/J-Plasma Precise Handpiece, Renuvion/J-Plasma Precise Open handpieces, Renuvion/J-Plasma Precise Open handpieces

  Class II

  FDA 510(k) K183610 Active Cleared 12 Mar 2019

• Bovie J-Plasma Precise Open handpiece & Bovie Ultimate Gen 2 High Frequency Electrosurgical Generator

  Class II

  FDA 510(k) K170188 Active Cleared 8 Mar 2017

• Bovie J-Plasma Precise 360 Handpiece

  Class II

  FDA 510(k) K152570 Active Cleared 2 Nov 2015

• Boss Coagulation Device, Model BOSS1215, Boss Coagulation Device, Angled Access, Model BOSA1215

  Class II

  FDA 510(k) K092149 Active Cleared 18 Mar 2010

See all devices from Bovie Medical Corporation →