What is FDA product code QVJ?

For the removal and destruction of skin lesions in general dermatological procedures, also referred to as Plasma Pen Devices, which generates electrical arc in the ambient air between an electrical probe tip and the skin and cause intended tissue damage for the removal and destruction of skin lesions

General & Plastic Surgery › SurgicalLow Power Electrosurgical Devices For Skin Lesion Destruction

Jett

Name: Jett
Brand: Jett

Catalogue number JETT PLASMA Medical II, listed by Compex, spol. s r.o., Czechia, under Low Power Electrosurgical Devices For Skin Lesion Destruction. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26

1manufacturer

1catalogue number

1510(k) clearance

Who Else Makes It

Registered in Guangdong.

Chinese manufacturers registered for FDA product code QVJ
Manufacturer	City	Province	Registered as	Device types
Shenzhen Leaflife Technology Co., Ltd.	Shenzhen	Guangdong	Manufacturer	5

Record

Regulatory record for Jett
Listed by	Compex, spol. s r.o., Czechia
FDA product code	QVJ
Device type	Low Power Electrosurgical Devices For Skin Lesion Destruction
Device class	Class 2
Regulation	21 CFR 878.4400
Establishment	Specification developer, Complaint-file establishment, Manufacturer
510(k)	K213247
Record published	2026-04-17

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Sterilisation	Liquid Chemical, Moist Heat or Steam Sterilization
Label carries	manufacturing date, serial number
Storage	Handling environment atmospheric pressure 50 to 106 KiloPascal; Handling environment humidity 30 to 70 % RH; Handling environment temperature 5 to 40 °C; Storage environment atmospheric pressure 50 to 106 KiloPascal; Storage environment humidity 30 to 70 % RH; Storage environment temperature 5 to 25 °C

Catalogue Numbers

Catalogue numbers for Jett
Catalogue number	Size	Status
JETT PLASMA Medical II		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
PlasmaMD	Med Pen Concepts LLC	2
Plasma+	Med Pen Concepts LLC	2
Mjolnir Pro.	Shenzhen Leaflife Technology Co., Ltd.	1
Plaxpot Multi Plasma	GCS Co., Ltd.	1

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance	Decision date
K213247	2023-03-14

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.