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Rhein83 S.r.l.

⚠️ Moderate Risk

FEI: 3002807996 • Bologna, Bologna • ITALY

FEI

FEI Number

3002807996

📍

Location

Bologna, Bologna

🇮🇹

Country

ITALY
🏢

Address

Via Emilio Zago 8, , Bologna, Bologna, Italy

Moderate Risk

FDA Import Risk Assessment

40.2
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

9
Total Refusals
3
Unique Violations
9/14/2015
Latest Refusal
6/17/2007
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
10.9×10%
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

5088×

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.

2372×

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).

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).

Refusal History

DateProductViolationsDivision
9/14/2015
76NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS
118NOT LISTED
508NO 510(K)
Cincinnati District Office (CIN-DO)
4/14/2014
76DZEIMPLANT, ENDOSSEOUS
508NO 510(K)
New York District Office (NYK-DO)
4/14/2014
76DZEIMPLANT, ENDOSSEOUS
508NO 510(K)
New York District Office (NYK-DO)
4/14/2014
76DZEIMPLANT, ENDOSSEOUS
508NO 510(K)
New York District Office (NYK-DO)
4/14/2014
76DZEIMPLANT, ENDOSSEOUS
508NO 510(K)
New York District Office (NYK-DO)
4/11/2014
76DZEIMPLANT, ENDOSSEOUS
508NO 510(K)
Cincinnati District Office (CIN-DO)
4/11/2014
76DZEIMPLANT, ENDOSSEOUS
508NO 510(K)
Cincinnati District Office (CIN-DO)
7/29/2009
76DZEIMPLANT, ENDOSSEOUS
237NO PMA
New York District Office (NYK-DO)
6/17/2007
76DZEIMPLANT, ENDOSSEOUS
237NO PMA
508NO 510(K)
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Rhein83 S.r.l.'s FDA import refusal history?

Rhein83 S.r.l. (FEI: 3002807996) has 9 FDA import refusal record(s) in our database, spanning from 6/17/2007 to 9/14/2015.

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. Rhein83 S.r.l.'s FEI number is 3002807996.

What types of violations has Rhein83 S.r.l. received?

Rhein83 S.r.l. 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 Rhein83 S.r.l. come from?

All FDA import refusal data for Rhein83 S.r.l. 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.