Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010923230

FEI Number

3010923230

Entity Name

VANTE, INC.

City/State/Country

Tucson, AZ, US

Establishment Address

3480 E Britannia Dr., Suite 120, Tucson, AZ 85706, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Vante, Inc. (Owner Number: 10054887)

Owner / Operator Contact Address

3480 E Britannia Dr., Suite 120, Tucson, AZ 85706, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SEBRA OMNI

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KSD	Device, Heat-Sealing	Hematology	Class 1	864.9750	2017-05-08

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vante, 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 3010923230. Last updated year: 2026. Please use registration number 3010923230 when referencing this establishment in official correspondence.