Lab.Pfortner Cornealent S.A
⚠️ Moderate Risk
FEI: 3005547688 • Ciudad Autonoma Buenos Aires, Buenos Aires • ARGENTINA
FEI Number
3005547688
Location
Ciudad Autonoma Buenos Aires, Buenos Aires
Country
ARGENTINAAddress
Avenida Pueyrredon 1706, , Ciudad Autonoma Buenos Aires, Buenos Aires, Argentina
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
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).
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 3/9/2006 | 86MVNLENS, CONTACT (DISPOSABLE) | Florida District Office (FLA-DO) | |
| 3/9/2006 | 86MVNLENS, CONTACT (DISPOSABLE) | Florida District Office (FLA-DO) | |
| 3/9/2006 | 86MVNLENS, CONTACT (DISPOSABLE) | Florida District Office (FLA-DO) | |
| 3/9/2006 | 86MVNLENS, CONTACT (DISPOSABLE) | Florida District Office (FLA-DO) |
Frequently Asked Questions
What is Lab.Pfortner Cornealent S.A's FDA import refusal history?
Lab.Pfortner Cornealent S.A (FEI: 3005547688) has 4 FDA import refusal record(s) in our database, spanning from 3/9/2006 to 3/9/2006.
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. Lab.Pfortner Cornealent S.A's FEI number is 3005547688.
What types of violations has Lab.Pfortner Cornealent S.A received?
Lab.Pfortner Cornealent S.A has been cited for 2 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 Lab.Pfortner Cornealent S.A come from?
All FDA import refusal data for Lab.Pfortner Cornealent S.A 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.