Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3004514095

FEI Number

3004514095

Entity Name

FLEX TECHNOLOGY INC.

City/State/Country

CHARLOTTESVILLE, VA, US

Establishment Address

801 WEST MAIN STREET, Suite 108, CHARLOTTESVILLE, VA 22903, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

FLEX TECHNOLOGY INC. (Owner Number: 9062757)

Owner / Operator Contact Address

801 WEST MAIN STREET, --, Charlottesville, VA 22903, US

Initial Importer Flag

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
HTO	Reamer	Orthopedic	Class 1	888.4540	2004-04-14

Official Correspondent

WILLIAM KRAUSE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FLEX TECHNOLOGY INC.

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0021-2015	Biomet, Inc.	1	Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor resections, revision of previously failed total joint arthroplasty, and trauma.

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9613926	Gesco Healthcare Private Limited	CHENNAI, Tamil Nadu, IN
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004514095. Last updated year: 2026. Please use registration number 3004514095 when referencing this establishment in official correspondence.