Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012971814

FEI Number

3012971814

Entity Name

The Flex Company

City/State/Country

Venice, CA, US

Establishment Address

318 Lincoln Blvd, Suite #204, Venice, CA 90291, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

The Flex Company (Owner Number: 10052408)

Owner / Operator Contact Address

318 Lincoln Blvd, Suite #204, Venice, CA 90291, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Flex Cup, Flex Disc, Softdisc, Softcup, Flex Reusable Disc, Flex Plant+ Disc

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHE	Cup, Menstrual	Obstetrics/Gynecology	Class 2	884.5400	2016-07-25

Official Correspondent

Panpan Wang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Flex Company

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 3012971814. Last updated year: 2026. Please use registration number 3012971814 when referencing this establishment in official correspondence.