WEVOTOPIA LLC

FDA Device Registration & Listing · Carpinteria, CA, US · Registration 3016421238

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3016421238
FEI Number
3016421238
Entity Name
WEVOTOPIA LLC
City/State/Country
Carpinteria, CA, US
Establishment Address
5425 Carpinteria Ave Unit #1146, Carpinteria, CA 93014, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Wevotopia LLC (Owner Number: 10061727)
Owner / Operator Contact Address
5425 Carpinteria Ave Unit #1146, Carpinteria, CA 93014, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kind Cup

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHE Cup, Menstrual Obstetrics/Gynecology Class 2 884.5400 2019-11-13

Official Correspondent

Christine Brown

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Wevotopia LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016421238. Last updated year: 2026. Please use registration number 3016421238 when referencing this establishment in official correspondence.
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