Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008161930

FEI Number

3008161930

Entity Name

CHRISTIE MEDICAL HOLDINGS, INC.

City/State/Country

Sanford, FL, US

Establishment Address

1201 Upsala Road, Sanford, FL 32771, US

Establishment Type(s)

Remanufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Christie Medical Holdings, Inc. (Owner Number: 10031287)

Owner / Operator Contact Address

1201 Upsala Road, Sanford, FL 32771, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VeinViewer Vision2 VeinViewer Flex

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KZA	Device, Vein Location, Liquid Crystal	General Hospital	Class 1	880.6970	2010-01-12

Official Correspondent

Salwa Rezk

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Christie Medical Holdings, Inc.

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 3008161930. Last updated year: 2026. Please use registration number 3008161930 when referencing this establishment in official correspondence.