BODY VISION MEDICAL LUNGVISION TOOL MANUFACTURING

FDA Device Registration & Listing · Netanya Northern, IL · Registration 3023214418

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
3023214418
FEI Number
3023214418
Entity Name
BODY VISION MEDICAL LUNGVISION TOOL MANUFACTURING
City/State/Country
Netanya Northern, IL
Establishment Address
4a H`azoran St., Netanya Northern 4250604, IL
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Body Vision Medical LungVision Tool Manufacturing (Owner Number: 10085426)
Owner / Operator Contact Address
4a H`azoran St, Netanya, IL-NOTA 4250604, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K172955
PMA Number
N/A

All Registered Proprietary Names

LungVison Tool

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 2022-06-16

Official Correspondent

No official correspondent registered.

US Agent Details

Matthew Dryden Business: ProMedic, LLC Email: matt.dryden@promedic.cc Phone: (239) 3076063

Related Public Records

Same Entity

Body Vision Medical LungVision Tool Manufacturing
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 3023214418. Last updated year: 2026. Please use registration number 3023214418 when referencing this establishment in official correspondence.
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