Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008436219

FEI Number

3008436219

Entity Name

JBC CORP

City/State/Country

Virginia Beach, VA, US

Establishment Address

552 Central Drive, Suite No. 110, Virginia Beach, VA 23454, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

JBC Corp (Owner Number: 10033382)

Owner / Operator Contact Address

552 Central Drive, Suite No. 110, Virginia Beach, VA 23454, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

JBC Nasopharyngeal 28FR JBC T-Ban Trauma Bandage JBC T-Ban XL Trauma Bandage JBC T-Ban Mini Trauma Bandage JBC T-Ban Type-C Trauma Bandage

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BTQ	Airway, Nasopharyngeal	Anesthesiology	Class 1	868.5100	2019-03-13
MHW	Dressing, Compression	General Hospital	Class 1	880.5075	2015-12-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

JBC Corp

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008436219. Last updated year: 2026. Please use registration number 3008436219 when referencing this establishment in official correspondence.