KIMBERLY-CLARK COSTA RICA, Ltda

FDA Device Registration & Listing · CARTAGO, CR · Registration 3005301318

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
3005301318
FEI Number
3005301318
Entity Name
KIMBERLY-CLARK COSTA RICA, Ltda
City/State/Country
CARTAGO, CR
Establishment Address
Detras del Parque Industrial Zeta 300m Oeste, Canton Central Distrito San Nicholas, CARTAGO --, CR
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device
Owner / Operator
KIMBERLY-CLARK CORPORATION (Owner Number: 9076467)
Owner / Operator Contact Address
1400 Holcomb Bridge Road, Roswell, GA 30076, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Kotex Esencial Kotex Nocturna

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 2005-08-15

Official Correspondent

No official correspondent registered.

US Agent Details

Wioletta Bauer Business: KIMBERLY-CLARK CORPORATION Email: wioletta.bauer@kcc.com Phone: (920) 7213132

Related Public Records

Same Entity

KIMBERLY-CLARK CORPORATION
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
9615625 KIMBERLY-CLARK PERSONAL HYGIENIC PRODUCTS CO.,LTD.BEIJING DEVELOPMENT ZONE, BEIJING, CN
3007697999 KIMBERLY-CLARK PERU S.R.L. - Santa Clara Mill Lima Lima (Region), PE
2184163 KIMBERLY-CLARK CORPORATION Cold Spring NEENAH, WI, US
1650783 KIMBERLY-CLARK CORPORATION PARIS PLANT PARIS, TX, US
3011109575 K-C AFC Manufacturing, S. de R.L. de C.V Nogales, Sonora Mexico, MX

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 3005301318. Last updated year: 2026. Please use registration number 3005301318 when referencing this establishment in official correspondence.
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