Nihon Kohden Corp.
⚠️ Moderate Risk
FEI: 3002807720 • Shinjuku, Tokyo • JAPAN
FEI Number
3002807720
Location
Shinjuku, Tokyo
Country
JAPANAddress
1 Chome 31-4, Nishiochiai, Shinjuku, Tokyo, Japan
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
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).
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 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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/16/2007 | 81JOXANALYZER, HEPARIN, AUTOMATED | 341REGISTERED | Florida District Office (FLA-DO) |
| 11/13/2006 | 74NPNDEFIBRILLATOR, AUTOMATIC, EXTERNAL, FOR OUT-OF-HOSPITAL USE | Florida District Office (FLA-DO) | |
| 11/13/2006 | 89ISBSTIMULATOR, MUSCLE, DIAGNOSTIC | Florida District Office (FLA-DO) | |
| 4/8/2005 | 74NPNDEFIBRILLATOR, AUTOMATIC, EXTERNAL, FOR OUT-OF-HOSPITAL USE | Division of Southeast Imports (DSEI) | |
| 1/26/2005 | 74DWSINSTRUMENTS, SURGICAL, CARDIOVASCULAR | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Nihon Kohden Corp.'s FDA import refusal history?
Nihon Kohden Corp. (FEI: 3002807720) has 5 FDA import refusal record(s) in our database, spanning from 1/26/2005 to 5/16/2007.
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. Nihon Kohden Corp.'s FEI number is 3002807720.
What types of violations has Nihon Kohden Corp. received?
Nihon Kohden Corp. has been cited for 3 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 Nihon Kohden Corp. come from?
All FDA import refusal data for Nihon Kohden Corp. 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.