MeKo Manufacturing e.K.
⚠️ Moderate Risk
FEI: 3009937642 • Sarstedt, Lower Saxony • GERMANY
FEI Number
3009937642
Location
Sarstedt, Lower Saxony
Country
GERMANYAddress
Im Kirchenfelde 12-14, , Sarstedt, Lower Saxony, Germany
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
NOT LISTED
It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
NO 510(K)
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.
FRNMFGREG
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.
REGISTERED
It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/9/2023 | 87KWFPROSTHESIS, FINGER, POLYMER | Division of Southeast Imports (DSEI) | |
| 5/24/2022 | 78PEWIMPLANTABLE TRANSPROSTATIC TISSUE RETRACTOR SYSTEM | Division of Southeast Imports (DSEI) | |
| 5/6/2020 | 79GBACATHETER, BALLOON TYPE | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 6/4/2019 | 78EZLCATHETER, RETENTION TYPE, BALLOON | Division of Southeast Imports (DSEI) | |
| 4/5/2019 | 80JOLCATHETER AND TIP, SUCTION | Division of Northern Border Imports (DNBI) | |
| 9/18/2017 | 74NIQSTENT, CORONARY, DRUG-ELUTING | Division of Southeast Imports (DSEI) | |
| 3/21/2017 | 74MAFSTENT, CARDIOVASCULAR | Division of Southeast Imports (DSEI) | |
| 9/26/2016 | 74NIOSTENT, ILIAC | Cincinnati District Office (CIN-DO) | |
| 9/9/2016 | 74NIOSTENT, ILIAC | 237NO PMA | Cincinnati District Office (CIN-DO) |
| 8/30/2016 | 74NIOSTENT, ILIAC | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 7/28/2016 | 74NIOSTENT, ILIAC | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 7/5/2016 | 74NIOSTENT, ILIAC | 118NOT LISTED | Cincinnati District Office (CIN-DO) |
| 6/8/2016 | 74NIOSTENT, ILIAC | Cincinnati District Office (CIN-DO) | |
| 5/31/2016 | 74NIOSTENT, ILIAC | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 4/1/2016 | 74NIOSTENT, ILIAC | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 11/20/2015 | 74NIOSTENT, ILIAC | 118NOT LISTED | Cincinnati District Office (CIN-DO) |
| 11/20/2015 | 74NIOSTENT, ILIAC | 118NOT LISTED | Cincinnati District Office (CIN-DO) |
| 3/1/2013 | 74NIOSTENT, ILIAC | 237NO PMA | New Orleans District Office (NOL-DO) |
| 6/20/2012 | 78LOADEVICE, TESTICULAR HYPOTHERMIA | 237NO PMA | New Orleans District Office (NOL-DO) |
| 6/11/2012 | 74NIPSTENT, SUPERFICIAL FEMORAL ARTERY | 237NO PMA | New Orleans District Office (NOL-DO) |
| 3/30/2012 | 74MAFSTENT, CARDIOVASCULAR | New Orleans District Office (NOL-DO) | |
| 6/8/2011 | 78KGCTUBE, GASTRO-ENTEROSTOMY | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 2/23/2011 | 74MAFSTENT, CARDIOVASCULAR | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 12/19/2008 | 78FADSTENT, URETERAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 2/2/2006 | 74MAFSTENT, CARDIOVASCULAR | 237NO PMA | New Orleans District Office (NOL-DO) |
| 12/16/2004 | 74MAFSTENT, CARDIOVASCULAR | 237NO PMA | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is MeKo Manufacturing e.K.'s FDA import refusal history?
MeKo Manufacturing e.K. (FEI: 3009937642) has 26 FDA import refusal record(s) in our database, spanning from 12/16/2004 to 3/9/2023.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. MeKo Manufacturing e.K.'s FEI number is 3009937642.
What types of violations has MeKo Manufacturing e.K. received?
MeKo Manufacturing e.K. has been cited for 5 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about MeKo Manufacturing e.K. come from?
All FDA import refusal data for MeKo Manufacturing e.K. is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.