FEMMEPHARMA CONSUMER HC, LLC

FDA Device Registration & Listing · Wayne, PA, US · Registration 3016931143

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
3016931143
FEI Number
3016931143
Entity Name
FEMMEPHARMA CONSUMER HC, LLC
City/State/Country
Wayne, PA, US
Establishment Address
175 STRAFFORD AVE BLDG 4 SUITE 275, Wayne, PA 19087, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
FemmePharma Consumer HC, LLC (Owner Number: 10074732)
Owner / Operator Contact Address
175 STRAFFORD AVE BLDG 4 SUITE 275, Wayne, PA 19087, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K190752
PMA Number
N/A

All Registered Proprietary Names

Satisfaite FemmePharma Mia Vita

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2020-05-29

Official Correspondent

Gerianne DiPiano

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FemmePharma Consumer HC, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K050212 Qualis, Inc. PERSONAL WARMING JELLY 2005-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016931143. Last updated year: 2026. Please use registration number 3016931143 when referencing this establishment in official correspondence.
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