Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043475715

FEI Number

3043475715

Entity Name

MENSE CO.

City/State/Country

San Luis Obispo, CA, US

Establishment Address

872 Higuera St, San Luis Obispo, CA 93401, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Mense Co. (Owner Number: 10095286)

Owner / Operator Contact Address

872 Higuera Street, San Luis Obispo, CA 93401, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Cove

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2026-02-18

Official Correspondent

McCall Brinskele

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Mense 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 3043475715. Last updated year: 2026. Please use registration number 3043475715 when referencing this establishment in official correspondence.