Maanshan Bond Medical Instruments Co., LTD.
⚠️ Moderate Risk
FEI: 3007699087 • Maanshan, Anhui • CHINA
FEI Number
3007699087
Location
Maanshan, Anhui
Country
CHINAAddress
Yushan 1358, 1358 Meishan Road; Yushan, Maanshan, Anhui, 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.
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 |
|---|---|---|---|
| 11/25/2019 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 341REGISTERED | Division of Northern Border Imports (DNBI) |
| 2/26/2016 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | Division of Southeast Imports (DSEI) | |
| 3/25/2015 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 2/17/2015 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
| 10/23/2014 | 80MQXNEEDLE, ACUPUNCTURE, SINGLE USE | 508NO 510(K) | Los Angeles District Office (LOS-DO) |
Frequently Asked Questions
What is Maanshan Bond Medical Instruments Co., LTD.'s FDA import refusal history?
Maanshan Bond Medical Instruments Co., LTD. (FEI: 3007699087) has 16 FDA import refusal record(s) in our database, spanning from 10/23/2014 to 11/25/2019.
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. Maanshan Bond Medical Instruments Co., LTD.'s FEI number is 3007699087.
What types of violations has Maanshan Bond Medical Instruments Co., LTD. received?
Maanshan Bond Medical Instruments Co., LTD. 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 Maanshan Bond Medical Instruments Co., LTD. come from?
All FDA import refusal data for Maanshan Bond Medical Instruments 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.