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GENIUS ORTHO PVT LTD

⚠️ Moderate Risk

FEI: 3013640617 • MENTODA • INDIA

FEI

FEI Number

3013640617

📍

Location

MENTODA

🇮🇳

Country

INDIA
🏢

Address

2019 G FAXTORY OPP RAJM, , MENTODA, , India

Moderate Risk

FDA Import Risk Assessment

29.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
1
Unique Violations
7/20/2017
Latest Refusal
7/20/2017
Earliest Refusal

Score Breakdown

Violation Severity
50.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

1183×

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).

Refusal History

DateProductViolationsDivision
7/20/2017
87LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
118NOT LISTED
Division of Southeast Imports (DSEI)
7/20/2017
87HRSPLATE, FIXATION, BONE
118NOT LISTED
Division of Southeast Imports (DSEI)
7/20/2017
87HWCSCREW, FIXATION, BONE
118NOT LISTED
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is GENIUS ORTHO PVT LTD's FDA import refusal history?

GENIUS ORTHO PVT LTD (FEI: 3013640617) has 3 FDA import refusal record(s) in our database, spanning from 7/20/2017 to 7/20/2017.

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. GENIUS ORTHO PVT LTD's FEI number is 3013640617.

What types of violations has GENIUS ORTHO PVT LTD received?

GENIUS ORTHO PVT LTD has been cited for 1 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 GENIUS ORTHO PVT LTD come from?

All FDA import refusal data for GENIUS ORTHO PVT LTD 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.