Syneron, Inc.
⚠️ Moderate Risk
FEI: 3004772125 • Irvine, CA • UNITED STATES
FEI Number
3004772125
Location
Irvine, CA
Country
UNITED STATESAddress
3 Goodyear Ste A, , Irvine, CA, United States
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
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).
NO REGISTR
The article appears to be an electronic product that does not comply with an applicable standard as prescribed by Section 534 because no reporting has been provided as required by Section 537(b).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 8/31/2018 | 79OUPPOWERED SURGICAL INSTRUMENTS FOR IMPROVEMENT IN THE APPEARANCE OF CELLULITE | Division of Southwest Imports (DSWI) | |
| 8/31/2018 | 79OHTLIGHT BASED OVER-THE-COUNTER HAIR REMOVAL | Division of Southwest Imports (DSWI) | |
| 8/31/2018 | 79OUPPOWERED SURGICAL INSTRUMENTS FOR IMPROVEMENT IN THE APPEARANCE OF CELLULITE | Division of Southwest Imports (DSWI) | |
| 8/31/2018 | 79ONGPOWERED LASER SURGICAL INSTRUMENT WITH MICROBEAM\FRACTIONAL OUTPUT | Division of Southwest Imports (DSWI) | |
| 8/31/2018 | 79ONGPOWERED LASER SURGICAL INSTRUMENT WITH MICROBEAM\FRACTIONAL OUTPUT | Division of Southwest Imports (DSWI) |
Frequently Asked Questions
What is Syneron, Inc.'s FDA import refusal history?
Syneron, Inc. (FEI: 3004772125) has 5 FDA import refusal record(s) in our database, spanning from 8/31/2018 to 8/31/2018.
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. Syneron, Inc.'s FEI number is 3004772125.
What types of violations has Syneron, Inc. received?
Syneron, Inc. 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 Syneron, Inc. come from?
All FDA import refusal data for Syneron, 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.