Silhouet-Tone Corporation
⚠️ Moderate Risk
FEI: 3005545844 • Laval, Quebec • CANADA
FEI Number
3005545844
Location
Laval, Quebec
Country
CANADAAddress
2185 Michelin St, , Laval, Quebec, Canada
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
NO PMA
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).
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 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.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
RX DEVICE
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.
FALSE
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose labeling appears to be false or misleading.
WARNINGS
It appears to lack adequate warning against use in a pathological condition or by children where it may be dangerous to health or against an unsafe dose, method, administering duration, application, in manner/form, to protect users.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
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).
COSM COLOR
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain a color additive which is unsafe within the meaning of Section 721(a) which renders it adulterated under Section 601(e).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 5/2/2019 | 95RHPUV LAMP, GERMICIDAL | Division of Northern Border Imports (DNBI) | |
| 3/23/2016 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 508NO 510(K) | New York District Office (NYK-DO) |
| 3/23/2016 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New York District Office (NYK-DO) |
| 1/10/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 79GFDDERMATOME | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 79GFDDERMATOME | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 79GFDDERMATOME | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 79GFDDERMATOME | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 79GFDDERMATOME | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 79GFDDERMATOME | 237NO PMA | New England District Office (NWE-DO) |
| 1/10/2014 | 79GFDDERMATOME | 237NO PMA | New England District Office (NWE-DO) |
| 11/19/2013 | 79PBXMASSAGER, VACUUM, RADIO FREQUENCY INDUCED HEAT | New England District Office (NWE-DO) | |
| 11/19/2013 | 79GFDDERMATOME | New England District Office (NWE-DO) | |
| 11/19/2013 | 89EGJDEVICE, IONTOPHORESIS, OTHER USES | New England District Office (NWE-DO) | |
| 11/19/2013 | 89EGJDEVICE, IONTOPHORESIS, OTHER USES | New England District Office (NWE-DO) | |
| 8/30/2013 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 118NOT LISTED | Detroit District Office (DET-DO) |
| 8/15/2013 | 89IMIDIATHERMY, ULTRASONIC, FOR USE IN APPLYING THERAPEUTIC DEEP HEAT | New England District Office (NWE-DO) | |
| 4/3/2013 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | 223FALSE | Detroit District Office (DET-DO) |
| 10/1/2012 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | Division of Southeast Imports (DSEI) | |
| 11/17/2005 | 53LD99OTHER SKIN CARE PREPARATIONS, N.E.C. | New York District Office (NYK-DO) | |
| 7/29/2005 | 89ISAMASSAGER, THERAPEUTIC, ELECTRIC | New York District Office (NYK-DO) |
Frequently Asked Questions
What is Silhouet-Tone Corporation's FDA import refusal history?
Silhouet-Tone Corporation (FEI: 3005545844) has 27 FDA import refusal record(s) in our database, spanning from 7/29/2005 to 5/2/2019.
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. Silhouet-Tone Corporation's FEI number is 3005545844.
What types of violations has Silhouet-Tone Corporation received?
Silhouet-Tone Corporation has been cited for 10 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 Silhouet-Tone Corporation come from?
All FDA import refusal data for Silhouet-Tone Corporation 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.