BHI IMPLANT
⚠️ Moderate Risk
FEI: 3010393542 • Afula, HA ZAFON • ISRAEL
FEI Number
3010393542
Location
Afula, HA ZAFON
Country
ISRAELAddress
2, Ha-Amal, , Afula, HA ZAFON, 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 |
|---|---|---|---|
| 12/12/2024 | 76NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 12/12/2024 | 76DZEIMPLANT, ENDOSSEOUS | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 12/12/2024 | 76NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 12/12/2024 | 76NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 12/12/2024 | 76NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 12/12/2024 | 76NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS | 341REGISTERED | Division of Southeast Imports (DSEI) |
| 12/12/2024 | 76NHAABUTMENT, IMPLANT, DENTAL, ENDOSSEOUS | 341REGISTERED | Division of Southeast Imports (DSEI) |
Frequently Asked Questions
What is BHI IMPLANT's FDA import refusal history?
BHI IMPLANT (FEI: 3010393542) has 7 FDA import refusal record(s) in our database, spanning from 12/12/2024 to 12/12/2024.
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. BHI IMPLANT's FEI number is 3010393542.
What types of violations has BHI IMPLANT received?
BHI IMPLANT 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 BHI IMPLANT come from?
All FDA import refusal data for BHI IMPLANT 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.