Arrow International, Inc. (Subsidiary of Teleflex, Inc.)
✅ Low Risk
FEI: 3015859709 • Wyomissing, PA • UNITED STATES
FEI Number
3015859709
Location
Wyomissing, PA
Country
UNITED STATESAddress
35 Innovation Way, , Wyomissing, PA, United States
Low Risk
FDA Import Risk Assessment
This firm has a minimal history of FDA import refusals with low-severity violations.
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
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).
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
Frequently Asked Questions
What is Arrow International, Inc. (Subsidiary of Teleflex, Inc.)'s FDA import refusal history?
Arrow International, Inc. (Subsidiary of Teleflex, Inc.) (FEI: 3015859709) has 1 FDA import refusal record(s) in our database, spanning from 2/26/2002 to 2/26/2002.
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. Arrow International, Inc. (Subsidiary of Teleflex, Inc.)'s FEI number is 3015859709.
What types of violations has Arrow International, Inc. (Subsidiary of Teleflex, Inc.) received?
Arrow International, Inc. (Subsidiary of Teleflex, Inc.) 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 Arrow International, Inc. (Subsidiary of Teleflex, Inc.) come from?
All FDA import refusal data for Arrow International, Inc. (Subsidiary of Teleflex, Inc.) 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.