HAYAT KIMYA A.S.

FDA Device Registration & Listing · Basiskele Kocaeli, TR · Registration 3015738552

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
3015738552
FEI Number
3015738552
Entity Name
HAYAT KIMYA A.S.
City/State/Country
Basiskele Kocaeli, TR
Establishment Address
Sepetlipinar Mahallesi, Hayat Caddesi, No. 2, Basiskele Kocaeli 41275, TR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Hayat Kimya A.S. (Owner Number: 10060990)
Owner / Operator Contact Address
Sepetlipinar Mahallesi, Hayat Caddesi, No. 2, Basiskele, TR-41 41275, TR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Menstrual Scented-Deodorized Pads Molped Menstrual Unscented Pad Molped

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2019-07-25
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2019-07-25
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2019-07-25

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Hayat Kimya A.S.
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 3015738552. Last updated year: 2026. Please use registration number 3015738552 when referencing this establishment in official correspondence.
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