JBC TECHNOLOGIES, INC.

FDA Device Registration & Listing · Elk Grove Village, IL, US · Registration 3038912598

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
3038912598
FEI Number
3038912598
Entity Name
JBC TECHNOLOGIES, INC.
City/State/Country
Elk Grove Village, IL, US
Establishment Address
1631 Brummel Ave, Elk Grove Village, IL 60007, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
JBC Technologies, Inc. (Owner Number: 10093701)
Owner / Operator Contact Address
1631 Brummel Avenue, Elk Grove Village, IL 60007, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2025-06-25

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JBC Technologies, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3006047460 JBC TECHNOLOGIES, INC. North Ridgeville, OH, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3038912598. Last updated year: 2026. Please use registration number 3038912598 when referencing this establishment in official correspondence.
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