INOVYTEC MEDICAL SOLUTIONS LTD
⚠️ Moderate Risk
FEI: 3017088380 • Ra'Anana • ISRAEL
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 9/26/2025 | 73CBKVENTILATOR, CONTINUOUS (RESPIRATOR) | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is INOVYTEC MEDICAL SOLUTIONS LTD's FDA import refusal history?
INOVYTEC MEDICAL SOLUTIONS LTD (FEI: 3017088380) has 1 FDA import refusal record(s) in our database, spanning from 9/26/2025 to 9/26/2025.
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. INOVYTEC MEDICAL SOLUTIONS LTD's FEI number is 3017088380.
What types of violations has INOVYTEC MEDICAL SOLUTIONS LTD received?
INOVYTEC MEDICAL SOLUTIONS LTD 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 INOVYTEC MEDICAL SOLUTIONS LTD come from?
All FDA import refusal data for INOVYTEC MEDICAL SOLUTIONS LTD 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.