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Mentor Texas, LP.

⚠️ Moderate Risk

FEI: 1000118360 • Irving, TX • UNITED STATES

FEI

FEI Number

1000118360

📍

Location

Irving, TX

🇺🇸
🏢

Address

3041 Skyway Cir N, , Irving, TX, United States

Moderate Risk

FDA Import Risk Assessment

47.3
LowModerateHighCritical

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

Statistics

8
Total Refusals
3
Unique Violations
12/1/2022
Latest Refusal
12/1/2022
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
35.3×30%
Recency
23.5×20%
Frequency
80.0×10%
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

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).

2378×

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).

32808×

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.

Refusal History

DateProductViolationsDivision
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)
12/1/2022
79FTRPROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED
118NOT LISTED
237NO PMA
3280FRNMFGREG
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Mentor Texas, LP.'s FDA import refusal history?

Mentor Texas, LP. (FEI: 1000118360) has 8 FDA import refusal record(s) in our database, spanning from 12/1/2022 to 12/1/2022.

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. Mentor Texas, LP.'s FEI number is 1000118360.

What types of violations has Mentor Texas, LP. received?

Mentor Texas, LP. has been cited for 3 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 Mentor Texas, LP. come from?

All FDA import refusal data for Mentor Texas, LP. 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.