KIMBERLY-CLARK CORPORATION (BEECH ISLAND MILL)

FDA Device Registration & Listing · BEECH ISLAND, SC, US · Registration 3005682435

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
3005682435
FEI Number
3005682435
Entity Name
KIMBERLY-CLARK CORPORATION (BEECH ISLAND MILL)
City/State/Country
BEECH ISLAND, SC, US
Establishment Address
246 OLD JACKSON HIGHWAY, BEECH ISLAND, SC 29842, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KIMBERLY-CLARK CORPORATION (Owner Number: 9001775)
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

Speax Thinx Poise Depend goodnites

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2007-03-09

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005682435. Last updated year: 2026. Please use registration number 3005682435 when referencing this establishment in official correspondence.
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