BECON MEDICAL Ltd.

FDA Device Registration & Listing · Batavia, IL, US · Registration 3006231901

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
3006231901
FEI Number
3006231901
Entity Name
BECON MEDICAL Ltd.
City/State/Country
Batavia, IL, US
Establishment Address
38W229 Grove Hill Court, Batavia, IL 60510, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
BECON MEDICAL, Ltd. (Owner Number: 9103543)
Owner / Operator Contact Address
38W229 Grove Hill Court, --, Batavia, IL 60510, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

EarWell Ear Correction Kit EarWell Ear Correction Splint

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FTN Plastic Surgery And Accessories Kit General, Plastic Surgery Class 1 878.3925 2009-06-16
NOC Splint, Extremity, Non-Inflatable, External, Non-Sterile General, Plastic Surgery Class 1 878.3910 2009-06-16

Official Correspondent

William Lyons

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BECON MEDICAL, Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006231901. Last updated year: 2026. Please use registration number 3006231901 when referencing this establishment in official correspondence.
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