Shenzhen Dongdixin Technology Co., Ltd.
⚠️ Moderate Risk
FEI: 3005170249 • Shenzhen, Guangdong • CHINA
FEI Number
3005170249
Location
Shenzhen, Guangdong
Country
CHINAAddress
Floor 1-2, No.3 Building, Fanshen Xusheng Industrial Estate Xilixiaobaimang, Nanshan District,, , 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).
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 |
|---|---|---|---|
| 5/23/2019 | 84GZJSTIMULATOR, NERVE, TRANSCUTANEOUS, FOR PAIN RELIEF | Division of Northern Border Imports (DNBI) | |
| 1/14/2010 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 341REGISTERED | Los Angeles District Office (LOS-DO) |
| 1/14/2010 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 341REGISTERED | Los Angeles District Office (LOS-DO) |
| 1/14/2010 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | Los Angeles District Office (LOS-DO) | |
| 9/14/2007 | 89MBQDEVICE, PERIPHERAL ELECTROMAGNETIC FIELD (PEMF) TO AID WOUND HEALING | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Shenzhen Dongdixin Technology Co., Ltd.'s FDA import refusal history?
Shenzhen Dongdixin Technology Co., Ltd. (FEI: 3005170249) has 5 FDA import refusal record(s) in our database, spanning from 9/14/2007 to 5/23/2019.
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. Shenzhen Dongdixin Technology Co., Ltd.'s FEI number is 3005170249.
What types of violations has Shenzhen Dongdixin Technology Co., Ltd. received?
Shenzhen Dongdixin Technology Co., Ltd. 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 Shenzhen Dongdixin Technology Co., Ltd. come from?
All FDA import refusal data for Shenzhen Dongdixin Technology Co., Ltd. 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.