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Sunny Medical Device (Shenzhen) Co., Ltd.

✅ Low Risk

FEI: 3007361214 • Shenzhen • CHINA

FEI

FEI Number

3007361214

📍

Location

Shenzhen

🇨🇳

Country

CHINA
🏢

Address

Zhongtianxin Bldg B F/1, Longgang, Shenzhen, , China

Low Risk

FDA Import Risk Assessment

21.8
LowModerateHighCritical

This firm has a minimal history of FDA import refusals with low-severity violations.

Statistics

2
Total Refusals
5
Unique Violations
3/21/2013
Latest Refusal
3/18/2009
Earliest Refusal

Score Breakdown

Violation Severity
40.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
5.0×10%
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

3412×

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).

1181×

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).

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

3351×

LACKS N/C

The article is in package form and appears to not have a label containing an accurate statement of the quantity of the contents in terms of weight, measure or numerical count and no variations or exemptions have been prescribed by regs.

5081×

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

DateProductViolationsDivision
3/21/2013
74DTLADAPTOR, STOPCOCK, MANIFOLD, FITTING, CARDIOPULMONARY BYPASS
118NOT LISTED
333LACKS FIRM
335LACKS N/C
341REGISTERED
508NO 510(K)
Los Angeles District Office (LOS-DO)
3/18/2009
79MDMINSTRUMENT, MANUAL, GENERAL SURGICAL
341REGISTERED
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Sunny Medical Device (Shenzhen) Co., Ltd.'s FDA import refusal history?

Sunny Medical Device (Shenzhen) Co., Ltd. (FEI: 3007361214) has 2 FDA import refusal record(s) in our database, spanning from 3/18/2009 to 3/21/2013.

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. Sunny Medical Device (Shenzhen) Co., Ltd.'s FEI number is 3007361214.

What types of violations has Sunny Medical Device (Shenzhen) Co., Ltd. received?

Sunny Medical Device (Shenzhen) Co., Ltd. has been cited for 5 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 Sunny Medical Device (Shenzhen) Co., Ltd. come from?

All FDA import refusal data for Sunny Medical Device (Shenzhen) 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.