SEKO MedTec Solutions

FDA Device Registration & Listing · Oakdale, PA, US · Registration 3010032952

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
3010032952
FEI Number
3010032952
Entity Name
SEKO MedTec Solutions
City/State/Country
Oakdale, PA, US
Establishment Address
300 Crown Court, Suite 320, Oakdale, PA 15071, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SEKO MedTec Solutions (Owner Number: 10042726)
Owner / Operator Contact Address
100 Walker Drive, State College, PA 16801, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ActaStim

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LQK Home Uterine Activity Monitor Obstetrics/Gynecology Class 2 884.2730 2021-07-20
LOF Stimulator, Bone Growth, Non-Invasive Orthopedic Class 2 890.5870 2021-01-22

Official Correspondent

No official correspondent registered.

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
3029833982 SEKO MEDTEC SOLUTIONS/SEKO Logistics Nashville Antioch, TN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010032952. Last updated year: 2026. Please use registration number 3010032952 when referencing this establishment in official correspondence.
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