Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012447313

FEI Number

3012447313

Entity Name

Viospex

City/State/Country

Parker, CO, US

Establishment Address

7647 E. Windlawn Way, Parker, CO 80134, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Viospex (Owner Number: 10051911)

Owner / Operator Contact Address

7647 E. Windlawn Way, Parker, CO 80134, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

The Bouquet Speculum

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HDL	Retractor, Vaginal	Obstetrics/Gynecology	Class 1	884.4520	2016-05-18

Official Correspondent

Jean Bouquet

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Viospex

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 3012447313. Last updated year: 2026. Please use registration number 3012447313 when referencing this establishment in official correspondence.