American Dental Systems
⚠️ Moderate Risk
FEI: 3003862567 • Vaterstetten, Bavaria • GERMANY
FEI Number
3003862567
Location
Vaterstetten, Bavaria
Country
GERMANYAddress
Johann-Sebastian-Bach-Str. 42, , Vaterstetten, Bavaria, Germany
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).
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.
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.
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).
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).
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 10/22/2021 | 79FTMMESH, SURGICAL | Division of Southeast Imports (DSEI) | |
| 12/18/2018 | 76EMOKNIFE, PERIODONTIC | Division of Southeast Imports (DSEI) | |
| 5/6/2016 | 74DXZPATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE | Division of Southeast Imports (DSEI) | |
| 5/6/2016 | 76EMOKNIFE, PERIODONTIC | Division of Southeast Imports (DSEI) | |
| 5/6/2016 | 76EMJELEVATOR, SURGICAL, DENTAL | Division of Southeast Imports (DSEI) | |
| 5/6/2016 | 76NDPACCESSORIES, IMPLANT, DENTAL, ENDOSSEOUS | Division of Southeast Imports (DSEI) | |
| 6/29/2015 | 76EJZKNIFE, MARGIN FINISHING, OPERATIVE | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 6/19/2015 | 79OVNSUTURE KIT | New Orleans District Office (NOL-DO) | |
| 6/19/2015 | 79OVNSUTURE KIT | New Orleans District Office (NOL-DO) | |
| 10/1/2014 | 79GAOSUTURE, NONABSORBABLE | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 79HTFCURETTE | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 76EMSCURETTE, PERIODONTIC | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 76EMSCURETTE, PERIODONTIC | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 76EMSCURETTE, PERIODONTIC | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 76EMSCURETTE, PERIODONTIC | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 79GDZHANDLE, SCALPEL | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 76EMSCURETTE, PERIODONTIC | New Orleans District Office (NOL-DO) | |
| 5/23/2014 | 76EMSCURETTE, PERIODONTIC | New Orleans District Office (NOL-DO) | |
| 4/2/2014 | 76DZNMATRIX, DENTAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 1/16/2014 | 79DZGSUTURE, DENTAL | New Orleans District Office (NOL-DO) | |
| 11/15/2013 | 78FHQHOLDER, NEEDLE | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 11/7/2013 | 87HXKHOLDER, NEEDLE; ORTHOPEDIC | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 9/5/2013 | 79GESBLADE, SCALPEL | New Orleans District Office (NOL-DO) | |
| 4/20/2012 | 79DZGSUTURE, DENTAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 4/20/2012 | 79GESBLADE, SCALPEL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 4/20/2012 | 76EMOKNIFE, PERIODONTIC | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 4/20/2012 | 79MDMINSTRUMENT, MANUAL, GENERAL SURGICAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 4/20/2012 | 79GESBLADE, SCALPEL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 4/20/2012 | 76EGNSCISSORS, SURGICAL TISSUE, DENTAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 4/20/2012 | 76EJBHANDLE, INSTRUMENT, DENTAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 8/22/2008 | 76ELWMATERIAL, IMPRESSION | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 12/18/2007 | 80LDQDEVICE, GENERAL MEDICAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 12/18/2007 | 80LDQDEVICE, GENERAL MEDICAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 12/18/2007 | 80LDQDEVICE, GENERAL MEDICAL | 118NOT LISTED | New Orleans District Office (NOL-DO) |
| 12/5/2007 | 76EMOKNIFE, PERIODONTIC | 118NOT LISTED | New Orleans District Office (NOL-DO) |
Frequently Asked Questions
What is American Dental Systems's FDA import refusal history?
American Dental Systems (FEI: 3003862567) has 35 FDA import refusal record(s) in our database, spanning from 12/5/2007 to 10/22/2021.
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. American Dental Systems's FEI number is 3003862567.
What types of violations has American Dental Systems received?
American Dental Systems 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 American Dental Systems come from?
All FDA import refusal data for American Dental Systems 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.