Edan Instruments, Inc.
⚠️ Moderate Risk
FEI: 3003971136 • Shenzhen, Guangdong • CHINA
FEI Number
3003971136
Location
Shenzhen, Guangdong
Country
CHINAAddress
Jinsha Comm., 15 Jinhui Road, Pingshan; Longgang, Shenzhen, Guangdong, China
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.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 1/23/2025 | 83PZFMERS-COV AND COMMON RESPIRATORY PATHOGENS MULTIPLEX NUCLEIC ACID DETECTION SYSTEM | Division of Southeast Imports (DSEI) | |
| 9/2/2021 | 90IYOSYSTEM, IMAGING, PULSED ECHO, ULTRASONIC | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 1/4/2021 | 85KNGMONITOR, ULTRASONIC, FETAL | Division of Southeast Imports (DSEI) | |
| 7/31/2018 | 74DPSELECTROCARDIOGRAPH | Division of West Coast Imports (DWCI) | |
| 7/31/2018 | 74DPSELECTROCARDIOGRAPH | Division of West Coast Imports (DWCI) | |
| 7/27/2018 | 74DPSELECTROCARDIOGRAPH | Division of West Coast Imports (DWCI) | |
| 1/22/2013 | 74DPSELECTROCARDIOGRAPH | 341REGISTERED | Florida District Office (FLA-DO) |
| 1/22/2013 | 74DPSELECTROCARDIOGRAPH | 341REGISTERED | Florida District Office (FLA-DO) |
| 1/22/2013 | 80KMIMONITOR, BED PATIENT | 341REGISTERED | Florida District Office (FLA-DO) |
| 1/22/2013 | 80KMIMONITOR, BED PATIENT | 341REGISTERED | Florida District Office (FLA-DO) |
| 3/19/2007 | 74DRTMONITOR, CARDIAC (INCL. CARDIOTACHOMETER & RATE ALARM) | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 10/14/2004 | 85LLTMONITOR, FETAL PH | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Edan Instruments, Inc.'s FDA import refusal history?
Edan Instruments, Inc. (FEI: 3003971136) has 12 FDA import refusal record(s) in our database, spanning from 10/14/2004 to 1/23/2025.
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. Edan Instruments, Inc.'s FEI number is 3003971136.
What types of violations has Edan Instruments, Inc. received?
Edan Instruments, Inc. has been cited for 4 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 Edan Instruments, Inc. come from?
All FDA import refusal data for Edan Instruments, Inc. 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.