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Tantus Inc

⚠️ Moderate Risk

FEI: 3005248387 • Sparks, NV • UNITED STATES

FEI

FEI Number

3005248387

📍

Location

Sparks, NV

🇺🇸
🏢

Address

1095 Spice Islands Dr Ste 100, , Sparks, NV, United States

Moderate Risk

FDA Import Risk Assessment

45.7
LowModerateHighCritical

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

Statistics

15
Total Refusals
5
Unique Violations
8/3/2016
Latest Refusal
3/31/2014
Earliest Refusal

Score Breakdown

Violation Severity
64.8×40%
Refusal Volume
44.6×30%
Recency
0.0×20%
Frequency
64.0×10%
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

1614×

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.

1184×

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).

5084×

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.

32802×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

2231×

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.

Refusal History

DateProductViolationsDivision
8/3/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
Division of Southeast Imports (DSEI)
7/25/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
New Orleans District Office (NOL-DO)
7/7/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
3280FRNMFGREG
508NO 510(K)
New Orleans District Office (NOL-DO)
7/7/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
New Orleans District Office (NOL-DO)
1/27/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
508NO 510(K)
Division of Southeast Imports (DSEI)
1/25/2016
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
508NO 510(K)
New Orleans District Office (NOL-DO)
12/11/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
Division of Southeast Imports (DSEI)
11/20/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
New Orleans District Office (NOL-DO)
11/17/2015
78FHWDEVICE, IMPOTENCE, MECHANICAL/HYDRAULIC
16DIRECTIONS
Division of Southeast Imports (DSEI)
4/24/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
Division of Southeast Imports (DSEI)
4/23/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
New Orleans District Office (NOL-DO)
3/20/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
223FALSE
New Orleans District Office (NOL-DO)
2/24/2015
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
Division of Southeast Imports (DSEI)
6/13/2014
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
118NOT LISTED
16DIRECTIONS
New Orleans District Office (NOL-DO)
3/31/2014
78LKYDEVICE, EXTERNAL PENILE RIGIDITY
16DIRECTIONS
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Tantus Inc's FDA import refusal history?

Tantus Inc (FEI: 3005248387) has 15 FDA import refusal record(s) in our database, spanning from 3/31/2014 to 8/3/2016.

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. Tantus Inc's FEI number is 3005248387.

What types of violations has Tantus Inc received?

Tantus Inc has been cited for 5 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 Tantus Inc come from?

All FDA import refusal data for Tantus 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.