Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029833982

FEI Number

3029833982

Entity Name

SEKO MEDTEC SOLUTIONS/SEKO Logistics Nashville

City/State/Country

Antioch, TN, US

Establishment Address

6050 Dana Way Ste 250, Antioch, TN 37013, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

SEKO MedTec Solutions (Owner Number: 10042726)

Owner / Operator Contact Address

100 Walker Drive, State College, PA 16801, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Breast Pump Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHH	Breast Pump Kit	Obstetrics/Gynecology	Class 2	884.5160	2024-11-14

Official Correspondent

John Traxler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SEKO MedTec Solutions

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3010032952	SEKO MedTec Solutions	Oakdale, PA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029833982. Last updated year: 2026. Please use registration number 3029833982 when referencing this establishment in official correspondence.