GENIAL DAY INC

FDA Device Registration & Listing · Bolingbrook, IL, US · Registration 3013478062

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
3013478062
FEI Number
3013478062
Entity Name
GENIAL DAY INC
City/State/Country
Bolingbrook, IL, US
Establishment Address
1115 Hosler Dr, Bolingbrook, IL 60490, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Genial Day INC (Owner Number: 10054604)
Owner / Operator Contact Address
1115 Hosler Dr., Bolingbrook, IL 60490, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Genial Day Genial Day

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 2019-04-19
HHE Cup, Menstrual Obstetrics/Gynecology Class 2 884.5400 2019-04-19

Official Correspondent

Vilmante Markeviciene

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Genial Day INC
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 3013478062. Last updated year: 2026. Please use registration number 3013478062 when referencing this establishment in official correspondence.
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