Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015526174

FEI Number

3015526174

Entity Name

FedEx Supply Chain, Inc.

City/State/Country

Columbus, OH, US

Establishment Address

9570 Logistics Court, Columbus, OH 43217, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

FedEx Supply Chain, Inc. (Owner Number: 10060829)

Owner / Operator Contact Address

145 Lt. George W. Lee Ave., Memphis, TN 38103, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PUMP, BREAST, NON-POWERED Pack, hot or cold, reusable UNIT, ULTRAVIOLET SANITATION/STERILIZATION (FOR TOOTHBRUSHES), NON-STERILE TOOTHBRUSH, POWERED UNIT, ORAL IRRIGATION

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HGY	Pump, Breast, Non-Powered	Obstetrics/Gynecology	Class 1	884.5150	2019-06-28
IME	Pack, Hot Or Cold, Reusable	Physical Medicine	Class 1	890.5700	2019-06-28
NOB	Unit, Ultraviolet Sanitation/Sterilization (For Toothbrushes), Non-Sterile	Dental	Class 1	872.6855	2020-09-21
JEQ	Toothbrush, Powered	Dental	Class 1	872.6865	2019-06-28
EFS	Unit, Oral Irrigation	Dental	Class 1	872.6510	2019-06-28

Official Correspondent

Joey Yopp

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FedEx Supply Chain, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3014197758	FEDEX SUPPLY CHAIN, INC.	Olive Branch, MS, US
3013403214	FedEx Supply Chain, Inc.	Memphis, TN, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K844318	Pro Pulse, Inc.	ORAL IRRIGATION TIP	1984-11-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015526174. Last updated year: 2026. Please use registration number 3015526174 when referencing this establishment in official correspondence.