AXESS VISION TECHNOLOGY

FDA Device Registration & Listing · Joue Les Tours Indre-et-Loire, FR · Registration 3017859830

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3017859830
FEI Number
3017859830
Entity Name
AXESS VISION TECHNOLOGY
City/State/Country
Joue Les Tours Indre-et-Loire, FR
Establishment Address
Zone de la Liodiere, 6 Rue De La Flottiere, Joue Les Tours Indre-et-Loire 37300, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
AXESS VISION TECHNOLOGY (Owner Number: 10079489)
Owner / Operator Contact Address
Zone de la Liodiere, 6 Rue de la Flottiere, Joue Les Tours, FR-37 37300, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Broncoflex Agile Screeni Broncoflex Vortex Broncoflex XFlo Broncoflex Agile Screeni Broncoflex Vortex

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EOQ Bronchoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4680 2022-07-22
EOQ Bronchoscope (Flexible Or Rigid) Ear, Nose, Throat Class 2 874.4680 2020-12-09

Official Correspondent

Federica FEDERICI

US Agent Details

Chris Duffie Business: TSC Life US Inc. Email: fda.tsclife-us@tsc-life.com Phone: (773) 5204980

Related Public Records

Same Entity

AXESS VISION TECHNOLOGY
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
K811059 Pentax Precision Instrument Corp. PENTAX BRONCHOFIBERSCOPE #FB-15A 1981-05-27
K142934 Covidien CrossCountry Transbronchial Access Tool straight, CrossCountry Transbronchial Access Tool curved 2015-06-17
K240075 FUJIFILM Healthcare Americas Corporation FUJIFILM Endoscope Model EB-710XT 2024-02-07

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0025-2020 AURIS HEALTH INC 2
Monarch, Aspirating Biopsy Needle, REF: MBR-000012, Rx Only, UDI: B634MBR0000120

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017859830. Last updated year: 2026. Please use registration number 3017859830 when referencing this establishment in official correspondence.
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