Jarvik Heart Inc
⚠️ Moderate Risk
FEI: 3003512469 • New York, NY • UNITED STATES
FEI Number
3003512469
Location
New York, NY
Country
UNITED STATESAddress
333 W 52nd St Fl 15, , New York, NY, United States
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
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).
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).
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).
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.
DV QUALITY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be adulterated since its strength differs from, or its purity or quality falls below, that which it purports or is represented to possess.
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.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/28/2018 | 74LOZHEART, ARTIFICIAL | Division of Northern Border Imports (DNBI) | |
| 4/28/2017 | 80LDQDEVICE, GENERAL MEDICAL | Division of Northern Border Imports (DNBI) | |
| 2/24/2014 | 74KFMPUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is Jarvik Heart Inc's FDA import refusal history?
Jarvik Heart Inc (FEI: 3003512469) has 3 FDA import refusal record(s) in our database, spanning from 2/24/2014 to 11/28/2018.
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. Jarvik Heart Inc's FEI number is 3003512469.
What types of violations has Jarvik Heart Inc received?
Jarvik Heart Inc has been cited for 6 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 Jarvik Heart Inc come from?
All FDA import refusal data for Jarvik Heart 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.