Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014193078

FEI Number

3014193078

Entity Name

NOVOXEL LTD.

City/State/Country

Netanya Tel Aviv, IL

Establishment Address

43 Hamelaha Street, Netanya Tel Aviv 4250573, IL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Novoxel Ltd. (Owner Number: 10080890)

Owner / Operator Contact Address

43 Hamelaha Street, Netanya, IL-TA 4250573, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K240512

PMA Number

N/A

All Registered Proprietary Names

T2 Cart Tixel I cart TC Cart Tixel System Tixel C Tixel® 2 System Tixel i

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BZN	Cart, Emergency, Cardiopulmonary (Excluding Equipment)	Anesthesiology	Class 1	868.6175	2023-07-03
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2021-03-04
GEI	Electrosurgical, Cutting & Coagulation & Accessories	General, Plastic Surgery	Class 2	878.4400	2023-07-03
ORZ	Eyelid Thermal Pulsation System	Ophthalmic	Class 2	886.5200	2024-11-25

Official Correspondent

Daniela Dov Elmaz

US Agent Details

Mindy McCann Business: Qserve Group US Inc. Email: usagent@qservegroup.com Phone: (424) 2718169

Related Public Records

Same Entity

Novoxel Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K970809	Somnus Medical Technologies, Inc.	BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL	1997-06-18
K222793	C.R. Bard, Inc.	WavelinQ Generator	2022-10-17
K002257	Tecno Instruments (Pvt.) , Ltd.	TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100	2000-10-19
K193591	Bowa-Electronics GmbH & Co. KG	ARC 400	2020-04-02
K192128	Sutter Medizintechnik GmbH	Sutter Arrowtip Monopolar Electrodes	2019-10-04

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-06	Rita Medical Systems	2	Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

Similar Registrations

Registration Number	Establishment Name	Location
3014256877	MULTIX SOLUTIONS S.R.L.	Mariano Comense Como, IT
3009750077	NANJING TIANAO MEDICAL INSTRUMENTS MANUFACTURE CO.,LTD	Nanjing Jiangsu, CN
3014270896	MOR-MEDICAL INTERNATIONAL	Pharr, TX, US
1937397	KOVEN TECHNOLOGY, INC.	Saint Louis, MO, US
3003882387	B. ALI IMPEX	SIALKOT, Punjab, PK

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014193078. Last updated year: 2026. Please use registration number 3014193078 when referencing this establishment in official correspondence.