Mydent International Shenzhen
⚠️ Moderate Risk
FEI: 3006768834 • Shenzhen, Guangdong • CHINA
FEI Number
3006768834
Location
Shenzhen, Guangdong
Country
CHINAAddress
Bldg 42 8a, Tao Yuan Road; Nanshan, 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
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 |
|---|---|---|---|
| 1/24/2011 | 76JEWTIP, RUBBER, ORAL HYGIENE | Chicago District Office (CHI-DO) | |
| 1/24/2011 | 76DYNMOUTHPIECE, SALIVA EJECTOR | Chicago District Office (CHI-DO) | |
| 1/24/2011 | 79EFQSPONGE, GAUZE | Chicago District Office (CHI-DO) |
Frequently Asked Questions
What is Mydent International Shenzhen's FDA import refusal history?
Mydent International Shenzhen (FEI: 3006768834) has 3 FDA import refusal record(s) in our database, spanning from 1/24/2011 to 1/24/2011.
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. Mydent International Shenzhen's FEI number is 3006768834.
What types of violations has Mydent International Shenzhen received?
Mydent International Shenzhen has been cited for 2 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 Mydent International Shenzhen come from?
All FDA import refusal data for Mydent International Shenzhen 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.