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Ortonense Equipamentos Hospitalares Ltda

⚠️ Moderate Risk

FEI: 3009192918 • Volta Redonda, Rio de Janeiro • BRAZIL

FEI

FEI Number

3009192918

📍

Location

Volta Redonda, Rio de Janeiro

🇧🇷

Country

BRAZIL
🏢

Address

Rua Coroados 67, , Volta Redonda, Rio de Janeiro, Brazil

Moderate Risk

FDA Import Risk Assessment

29.5
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
3/4/2013
Latest Refusal
2/6/2012
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
27.9×10%
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

1183×

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).

5083×

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.

37412×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(o) in that it is being imported or offered for import into the United States, and the importer, owner, or consignee of such article did not, at the time of offering the article for import, submit to the Secretary a statement that identifies the registration under section 510(i) of the Act of each establishment that with respect to such article is required under such section to register with the Secretary.

3411×

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).

Refusal History

DateProductViolationsDivision
3/4/2013
79NEHANCHOR, FASCIAL
118NOT LISTED
3741FRNMFGREG
508NO 510(K)
Florida District Office (FLA-DO)
3/4/2013
79NEHANCHOR, FASCIAL
118NOT LISTED
3741FRNMFGREG
508NO 510(K)
Florida District Office (FLA-DO)
2/6/2012
87LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
118NOT LISTED
341REGISTERED
508NO 510(K)
Florida District Office (FLA-DO)

Frequently Asked Questions

What is Ortonense Equipamentos Hospitalares Ltda's FDA import refusal history?

Ortonense Equipamentos Hospitalares Ltda (FEI: 3009192918) has 3 FDA import refusal record(s) in our database, spanning from 2/6/2012 to 3/4/2013.

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. Ortonense Equipamentos Hospitalares Ltda's FEI number is 3009192918.

What types of violations has Ortonense Equipamentos Hospitalares Ltda received?

Ortonense Equipamentos Hospitalares Ltda 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 Ortonense Equipamentos Hospitalares Ltda come from?

All FDA import refusal data for Ortonense Equipamentos Hospitalares Ltda 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.