HEMPRESS HYGIENICS

FDA Device Registration & Listing · Wilmington, DE, US · Registration 3027388272

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
3027388272
FEI Number
3027388272
Entity Name
HEMPRESS HYGIENICS
City/State/Country
Wilmington, DE, US
Establishment Address
919 North Market St, Suite 950, Wilmington, DE 19801, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Hempress Hygienics (Owner Number: 10087893)
Owner / Operator Contact Address
919 North Market St, Suite 950, Wilmington, DE 19801, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Hempress Hygienics Liners Hempress Hygienics Overnight Pads Hempress Hygienics Super Pads Hempress Hygienics Regular Pads

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2026-06-15

Official Correspondent

Marilyn Califano

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hempress Hygienics
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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027388272. Last updated year: 2026. Please use registration number 3027388272 when referencing this establishment in official correspondence.
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