MeKo Manufacturing e.K.

FDA Device Registration & Listing · Sarstedt Lower Saxony, DE · Registration 3009937642

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
3009937642
FEI Number
3009937642
Entity Name
MeKo Manufacturing e.K.
City/State/Country
Sarstedt Lower Saxony, DE
Establishment Address
Im Kirchenfelde 12-14, Sarstedt Lower Saxony 31157, DE
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
MeKo Manufacturing e.K. (Owner Number: 10044323)
Owner / Operator Contact Address
Im Kirchenfelde 12-14, Sarstedt, DE-NI 31157, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
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
PRL Iliac Covered Stent, Arterial Unknown Class 3 N/A 2017-07-14

Official Correspondent

No official correspondent registered.

US Agent Details

Tim Fries Business: MeKo MedTech Inc Email: tim.fries@meko-medtech.com Phone: (612) 2409392

Related Public Records

Same Entity

MeKo Manufacturing e.K.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0024-2025 Atrium Medical Corporation 3
iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009937642. Last updated year: 2026. Please use registration number 3009937642 when referencing this establishment in official correspondence.
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