Lena Cup

FDA Device Registration & Listing · New York, NY, US · Registration 3011390138

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
3011390138
FEI Number
3011390138
Entity Name
Lena Cup
City/State/Country
New York, NY, US
Establishment Address
244 5th Ave Unit 2243, New York, NY 10001, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Lena Cup LLC (Owner Number: 10048659)
Owner / Operator Contact Address
244 5th Avenue, #2243, New York, NY 10001, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

LENA cup lena LENA menstrual cup Lena Cup Lenacup LENA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHE Cup, Menstrual Obstetrics/Gynecology Class 2 884.5400 2015-02-09

Official Correspondent

Vilislava Petrova

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Lena Cup LLC
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 3011390138. Last updated year: 2026. Please use registration number 3011390138 when referencing this establishment in official correspondence.
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