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AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001)

Aventix Medical, Inc.

Country / Region:United States (US)Submission type:Traditional

Product code GEI· 21 CFR 878.4400

Summary PDF

Company

United States (US)

Product code

GEI
21 CFR 878.4400

Predicate devices

2

Cited as predicate

0

Device details

FDA 510(k) registration fields

K number
K260255
Device name
AVENTIX PFX System (PFX01); NOVOCLEAR Device (CLR001)
Country / Region
United States(US)
Product code
GEI
Device class
Class 2
Regulation number
21 CFR 878.4400
Date received
2026-01-28
Decision date
2026-03-27
Submission type
Traditional
Technology type
RF Ablation(AI inferred)
Clinical applications
SurgeryPain Management
Primary application
Surgery
Classification source
AI classified

Indications for Use

The AVENTIX™ PFX System is indicated for use in small clinics, offices and/or hospital environments. The NOVOCLEAR™ Device is indicated for use in otorhinolaryngology (ENT) surgery for the destruction of soft tissue in the nasal airway, including the posterior nasal nerve distribution in patients with chronic rhinitis.

Intended Use

The AVENTIX™ PFX System is an electrosurgical system intended to generate pulsed field energy (PFE) for use with the NOVOCLEAR™ Device. The AVENTIX™ PFX System is indicated for use in small clinics, offices and/or hospital environments. The NOVOCLEAR™ Device is indicated for use in otorhinolaryngology (ENT) surgery for the destruction of soft tissue in the nasal airway, including the posterior nasal nerve distribution in patients with chronic rhinitis.

Device Description

The AVENTIX™ PFX System and NOVOCLEAR™ Device include the following components: 1) NOVOCLEAR™ Device - a single use, hand-held device capable of delivering pulsed field energy (PFE) to targeted tissue. The NOVOCLEAR™ Device consists of a handle, a dome-like electrode and an electrical connector. The dome-like electrode delivers PFE and is angled to approximately 60 degrees, to aid access to the targeted tissue. An electrical connector is used to connect the NOVOCLEAR™ Device to the AVENTIX™ Generator. 2) AVENTIX™ Generator - generates predefined PFE output, which is delivered to the NOVOCLEAR™ Device dome-like electrode tip. 3) AVENTIX™ Controller – Performs validation of the NOVOCLEAR™ Device prior to use, changes the status of the Generator between armed and disarmed, and receives and displays parameters from the generator to the user. 4) Footswitch – for selective activation by the user to initiate PFE output. The NOVOCLEAR™ Device delivers pulsed field energy (PFE) to soft tissues in the nasal airway, including the posterior nasal nerve distribution. Non-clinical testing was performed to support safety and performance for the labeled use.

Summary parsed at:2026-06-19 06:03:41 UTC

Predicate devices

2

K260255 references 2 predicate/reference devices

Cited as predicate

0

No later 510(k)s cite this device yet

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