Pro-Dex Inc
✅ Low Risk
FEI: 2081135 • Irvine, CA • UNITED STATES
FEI Number
2081135
Location
Irvine, CA
Country
UNITED STATESAddress
2361 Mcgaw Ave, , Irvine, CA, 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
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
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/17/2020 | 79GEYMOTOR, SURGICAL INSTRUMENT, AC-POWERED | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is Pro-Dex Inc's FDA import refusal history?
Pro-Dex Inc (FEI: 2081135) has 1 FDA import refusal record(s) in our database, spanning from 4/17/2020 to 4/17/2020.
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. Pro-Dex Inc's FEI number is 2081135.
What types of violations has Pro-Dex Inc received?
Pro-Dex Inc has been cited for 1 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 Pro-Dex Inc come from?
All FDA import refusal data for Pro-Dex 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.