DAYE (ANNE'S DAY LTD)

FDA Device Registration & Listing · London London, City of, GB · Registration 3036679730

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
3036679730
FEI Number
3036679730
Entity Name
DAYE (ANNE'S DAY LTD)
City/State/Country
London London, City of, GB
Establishment Address
4th Floor, 22 Southwark Bridge Road,, London London, City of SE1 9HF, GB
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Daye (Anne's Day Ltd) (Owner Number: 10088636)
Owner / Operator Contact Address
100 Drummond Road, London, GB-LND SE16 4DG, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Daye Hemp Pads Daye Vaginal Tampon Swab Daye at-Home Microbiome Screening Vaginal Microbiome Test Daye at-Home Vaginal Microbiome Screen

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 2024-10-14
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2024-07-23

Official Correspondent

Kavita Blaggan

US Agent Details

Emily Matorin Business: FDAbasics LLC Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Daye (Anne's Day Ltd)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3028725772 Tampon Innovations Sofia Sofia-Grad, BG

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 3036679730. Last updated year: 2026. Please use registration number 3036679730 when referencing this establishment in official correspondence.
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