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Silhouet-Tone Corporation

⚠️ Moderate Risk

FEI: 3005545844 • Laval, Quebec • CANADA

FEI

FEI Number

3005545844

📍

Location

Laval, Quebec

🇨🇦

Country

CANADA
🏢

Address

2185 Michelin St, , Laval, Quebec, Canada

Moderate Risk

FDA Import Risk Assessment

45.5
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

27
Total Refusals
10
Unique Violations
5/2/2019
Latest Refusal
7/29/2005
Earliest Refusal

Score Breakdown

Violation Severity
68.5×40%
Refusal Volume
53.6×30%
Recency
0.0×20%
Frequency
19.6×10%
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

23715×

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).

1188×

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).

5087×

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.

163×

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.

842×

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.

2232×

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.

3441×

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.

4731×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

3411×

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).

1971×

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

DateProductViolationsDivision
5/2/2019
95RHPUV LAMP, GERMICIDAL
118NOT LISTED
344WARNINGS
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
118NOT LISTED
508NO 510(K)
New England District Office (NWE-DO)
11/19/2013
79GFDDERMATOME
118NOT LISTED
508NO 510(K)
New England District Office (NWE-DO)
11/19/2013
89EGJDEVICE, IONTOPHORESIS, OTHER USES
118NOT LISTED
16DIRECTIONS
508NO 510(K)
84RX DEVICE
New England District Office (NWE-DO)
11/19/2013
89EGJDEVICE, IONTOPHORESIS, OTHER USES
118NOT LISTED
16DIRECTIONS
508NO 510(K)
84RX DEVICE
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
118NOT LISTED
223FALSE
508NO 510(K)
New England District Office (NWE-DO)
4/3/2013
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
223FALSE
Detroit District Office (DET-DO)
10/1/2012
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)
11/17/2005
53LD99OTHER SKIN CARE PREPARATIONS, N.E.C.
197COSM COLOR
473LABELING
New York District Office (NYK-DO)
7/29/2005
89ISAMASSAGER, THERAPEUTIC, ELECTRIC
118NOT LISTED
16DIRECTIONS
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.