Argen Corporation
Argen Corporation appears in FDA public data with 0 recalls, 11 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Oct 24, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 11
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K242458 | ArgenZ MTZ | Oct 24, 2024 |
| K192846 | Argen Clear Aligner, Argen Clear Aligner Premium | Feb 10, 2020 |
| K183229 | Argen Clear Aligner | Jun 7, 2019 |
| K190079 | ArgenZ HT+ | Apr 12, 2019 |
| K182833 | ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer | Feb 8, 2019 |
| K172430 | ArgenIS Titanium Abutments | May 18, 2018 |
| K160248 | ArgenIS Titanium Abutments | Aug 5, 2016 |
| K143051 | ArgenIS Titanium Abutments | Sep 16, 2015 |
| K150919 | ArgenZ Esthetic Plus | Jul 13, 2015 |
| K140894 | ARGEN PMMA | Jul 31, 2014 |
| K071410 | ARGEN PEARL BRAND ZIRCONIA | Aug 15, 2007 |