D-23 Denture Adhesive
FDA 510(k) K871980 · Solar Dental Co., Inc.
510(k) numberK871980
Submission
- Device name
- D-23 Denture Adhesive
- Applicant
- Solar Dental Co., Inc.
Chicago, IL, US - Received
- May 22, 1987
- Decision date
- June 5, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code KOJ
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K251425 | turbodent touchKOJ · Traditional | Mectron S.P.A. | 05/09/2025SE |
| K063236 | Beta-PowderKOJ · Traditional | Brainbase Corporation | 02/16/2007SE |
| K042872 | Rondoflex Plus 360KOJ · Special | Kavo America Corporation | 11/23/2004SE |
| K033675 | Prosmile Air Polisher and Prophylaxis PowderKOJ · Traditional | Sirona Dental Systems GmbH | 01/15/2004SE |
| K033215 | PrepairKOJ · Traditional | Danville Materials, Inc. | 01/09/2004SE |
| K024105 | Velopex Aquacut Fluid Abrasion UnitKOJ · Traditional | Velopex International, Inc. | 10/09/2003SE |
| K030292 | Groman PrepmasterKOJ · Traditional | Groman, Inc. | 04/15/2003SE |
| K021450 | Clinpro Prophy PowderKOJ · Traditional | 3M Espe AG Dental Products | 08/01/2002SE |
| K014188 | New Prophy PowderKOJ · Traditional | Dentsply Intl. | 03/15/2002SE |
| K014252 | JetstreamKOJ · Traditional | Deldent , Ltd. | 02/19/2002SE |
More from Deldent , Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K861846 | Hydron Root Canal Filling & Mark IV Starter KitEIC · Traditional | 06/26/1986SE |
| K852926 | Dentolock II Denture Adhesive Cream · Traditional | 08/23/1985SE |
| K831294 | Solarcry/Temporary Crown & Bridge MatEBG · Traditional | 08/31/1983SE |
| K831293 | Solarcryl Custom Tray MaterialEBH · Traditional | 07/26/1983SE |
| K831265 | Dentolock Denture Adhesive CreamKOQ · Traditional | 05/09/1983SE |
Questions and answers
When was D-23 Denture Adhesive cleared by the FDA?
D-23 Denture Adhesive (K871980) received a 510(k) decision of Substantially Equivalent on June 5, 1987, 14 days after the submission was received.
What is the product code of K871980?
The FDA product code is KOJ – Airbrush, a Class II (moderate risk) device regulated under 21 CFR 872.6080.