YILSON MEDICAL TECHNOLOGY CO
⚠️ Moderate Risk
FEI: 3013768882 • Shenzhen • CHINA
FEI Number
3013768882
Location
Shenzhen
Country
CHINAAddress
5/F, Fuxuan Building, 28 East Heping Road, Shenzhen, , 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
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.
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).
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 |
|---|---|---|---|
| 3/3/2020 | 74DYBINTRODUCER, CATHETER | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74OEQANGIOGRAPHY/ANGIOPLASTY KIT | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74PTLWIRE, GUIDE, CATHETER, EXEMPT | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74PTLWIRE, GUIDE, CATHETER, EXEMPT | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74DYBINTRODUCER, CATHETER | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74PTLWIRE, GUIDE, CATHETER, EXEMPT | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74DYBINTRODUCER, CATHETER | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74DYBINTRODUCER, CATHETER | Division of West Coast Imports (DWCI) | |
| 3/3/2020 | 74DYBINTRODUCER, CATHETER | Division of West Coast Imports (DWCI) | |
| 7/22/2019 | 80FRNPUMP, INFUSION | Division of Southeast Imports (DSEI) | |
| 5/28/2019 | 78FADSTENT, URETERAL | 118NOT LISTED | Division of Southeast Imports (DSEI) |
| 6/15/2018 | 74OFLPERCUTANEOUS SHEATH INTRODUCER KIT | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is YILSON MEDICAL TECHNOLOGY CO's FDA import refusal history?
YILSON MEDICAL TECHNOLOGY CO (FEI: 3013768882) has 12 FDA import refusal record(s) in our database, spanning from 6/15/2018 to 3/3/2020.
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. YILSON MEDICAL TECHNOLOGY CO's FEI number is 3013768882.
What types of violations has YILSON MEDICAL TECHNOLOGY CO received?
YILSON MEDICAL TECHNOLOGY CO 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 YILSON MEDICAL TECHNOLOGY CO come from?
All FDA import refusal data for YILSON MEDICAL TECHNOLOGY CO 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.