PROCTER & GAMBLE DISTRIBUTING LLC, THE

FDA Device Registration & Listing · Union, OH, US · Registration 3011964664

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
3011964664
FEI Number
3011964664
Entity Name
PROCTER & GAMBLE DISTRIBUTING LLC, THE
City/State/Country
Union, OH, US
Establishment Address
1800 UNION AIRPARK BLVD, Union, OH 45377, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Procter & Gamble (Owner Number: 9915005)
Owner / Operator Contact Address
1 PROCTER & GAMBLE PLAZA, --, Cincinnati, OH 45202, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NXZ Dental Hygiene Kit Dental Class 1 872.6855 2015-08-17
HEB Tampon, Menstrual, Unscented Obstetrics/Gynecology Class 2 884.5470 2012-04-04
EEG Heat Source For Bleaching Teeth Dental Class 1 872.6475 2016-11-07
OHT Light Based Over-The-Counter Hair Removal General, Plastic Surgery Class 2 878.4810 2019-12-18
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2019-12-18
HEB Tampon, Menstrual, Unscented Obstetrics/Gynecology Class 2 884.5470 2014-04-16
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 1987-12-31
KOO Adhesive, Denture, Polyvinyl Methylether Maleic Acid Calcium-Sodium Double Salt Dental Class 1 872.3490 1997-04-10
ONF Powered Light Based Non-Laser Surgical Instrument With Thermal Effect General, Plastic Surgery Class 2 878.4810 2015-12-22
OHT Light Based Over-The-Counter Hair Removal General, Plastic Surgery Class 2 878.4810 2015-12-22
GEX Powered Laser Surgical Instrument General, Plastic Surgery Class 2 878.4810 2015-12-22
JEW Tip, Rubber, Oral Hygiene Dental Class 1 872.6650 2007-12-07
HHE Cup, Menstrual Obstetrics/Gynecology Class 2 884.5400 2018-09-06
JET Pick, Massaging Dental Class 1 872.6650 2007-12-06
EFT Cleanser, Denture, Over The Counter Dental Class 1 872.3520 1998-11-30
EFW Toothbrush, Manual Dental Class 1 872.6855 2001-07-30
LCN Scraper, Tongue Dental Class 1 872.6855 2007-12-06
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 1986-11-26
JES Floss, Dental Dental Class 1 872.6390 1997-03-27
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2004-07-12
HIL Tampon, Menstrual, Scented, Scented-Deodorized Obstetrics/Gynecology Class 2 884.5460 2012-04-04
HEB Tampon, Menstrual, Unscented Obstetrics/Gynecology Class 2 884.5470 2012-04-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Procter & Gamble
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1062366 PROCTER & GAMBLE CO. Brown Summit, NC, US
3000302531 Procter & Gamble Manufacturing GmbH MARKTHEIDENFELD Bavaria, DE
3007817025 Gillette Diversified Operations (P) Ltd Mumbai Maharashtra, IN
3013504555 Procter & Gamble Hyginett Kft. Gyongyos Heves, HU
2521156 PROCTER AND GAMBLE MFG CO MEHOOPANY PLANT Mehoopany, PA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K923985 Personal Products Co. UNSCENTED MENSTRUAL TAMPON 1993-02-19
K151170 Tosama, D.O.O. Tosama 100% Organic Cotton Menstrual Tampon 2015-07-02
K930149 Kimberly-Clark Corp. KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+ 1994-03-02
K083258 Dornier Medtech America, Inc. MEDILAS D FAMILY LASERS, INCLUDING MEDILAS D LITEBEAM, LITEBEAM +, UROBEAM, MULTIBEAM, FLEXIPULSE AND MAGNAPULSE 2009-01-30
K201111 Candela Corporation GentleMax Pro Plus 2020-05-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0005-2014 PhotoMedex, Inc. 2
The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product Number 0041-3082; SLT-SSRH 11, Catalog/Product Number 0041-3112; SLT-SSRH 4-SMA, Catalog/Product Number 0042-0075; SLT-SSRH 5-SMA, Catalog/Product Number 0042-0076; SLT-SSRH 6-SMA, Catalog/Product Number 0042-0077; SLT-SSRH 7-SMA, Catalog/Product Number 0042-0078; SLT-SSRH 8-SMA, Catalog/Product Number 0042-0079; SLT-SSRH 9-SMA, Catalog/Product Number 0041-4931; and SLT-SSRH 10-SMA, Catalog/Product Number 0042-0081. Indicated for the incision, excision, coagulations, and vaporization of soft tissue.
Z-0025-2018 Medtronic Navigation, Inc. 2
VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
Z-0028-2007 Lumenis Inc. 2
Lumenis brand DuoTome SideLite 550 Micron Delivery System; laser systems for ablating soft tissue. Catalog Number: 0641-800-01; Manufactured by Lumenis, Inc., 2400 Condensa Street, Santa Clara, CA

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011964664. Last updated year: 2026. Please use registration number 3011964664 when referencing this establishment in official correspondence.
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