Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1010842

FEI Number

1010842

Entity Name

BARNHARDT MFG. CO.

City/State/Country

CHARLOTTE, NC, US

Establishment Address

1100 Hawthorne Ln, CHARLOTTE, NC 28205, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

BARNHARDT MFG. CO. (Owner Number: 1010842)

Owner / Operator Contact Address

1100 HAWTHORNE LN., PO Box 34276 Zip 28234, Charlotte, NC 28205, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ABSORBENT FIBER

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FRL	Fiber, Medical, Absorbent	General Hospital	Class 1	880.5300	2007-03-29

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BARNHARDT MFG. CO.

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 1010842. Last updated year: 2026. Please use registration number 1010842 when referencing this establishment in official correspondence.