MVLUnclassified
Cord, Retraction
Unknown
MVL is the FDA product code for Cord, Retraction. As of , FDA records hold 36 510(k) clearances under this code, the most recent dated , and one recall.
Classification record
- Product code
- MVL
- Device name
- Cord, Retraction
- Device class
- Unclassified
- Review panel
- Unknown
- Submission type
- 510(k)
- Implant
- No
- Life sustaining or supporting
- No
- GMP exempt
- No
- Third party review eligible
- No
- Ingested clearances
- 36
- Ingested recalls
- 1
Clearances, product code MVL
By decision yearShow the numbers
| Year | Clearances |
|---|---|
| 1998 | 1 |
| 2001 | 1 |
| 2004 | 1 |
| 2005 | 1 |
| 2006 | 1 |
| 2008 | 1 |
| 2009 | 3 |
| 2010 | 4 |
| 2011 | 2 |
| 2012 | 1 |
| 2013 | 2 |
| 2014 | 2 |
| 2015 | 2 |
| 2017 | 4 |
| 2018 | 1 |
| 2019 | 1 |
| 2020 | 2 |
| 2021 | 1 |
| 2022 | 2 |
| 2025 | 1 |
| 2026 | 2 |
Applicants with the most clearances
Product code MVL| Applicant | Clearances |
|---|---|
| Sybron Dental Specialties, Inc. | 5 |
| Ultradent Products Inc. | 4 |
| Centrix, Inc. | 3 |
| Belport Company, Inc., Gingi-Pak | 2 |
| Inter-Med/Vista Dental Products | 2 |
| Premier Dental Products Co | 2 |
| Produits Dentaires Pierre Rolland | 2 |
| 3M Espe AG Dental Products | 1 |
| Biotech One, Inc. | 1 |
| Centrix Incorporated | 1 |
Companies listing this code with FDA
Companies whose registered establishments list this codeFIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.