Isopast-Ds
FDA 510(k) K802680 · Vivadent (Usa), Inc.
510(k) numberK802680
Submission
- Device name
- Isopast-Ds
- Applicant
- Vivadent (Usa), Inc.
Mchenry, IL, US - Received
- October 28, 1980
- Decision date
- November 12, 1980
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Other 510(k)s with product code EBF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262202 | Cerasmart ForteEBF · Traditional | GC America, Inc. | 09/10/2026SE |
| K261695 | Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)EBF · Traditional | Guilin Kevin Peter Technology Co., Ltd. | 08/31/2026SE |
| K262228 | Transcend Bulk Fill Flowable CompositeEBF · Traditional | Ultradent Products, Inc. | 07/01/2026SE |
| K261485 | Tetric plus Fill;Tetric plus FlowEBF · Traditional | Ivoclar Vivadent, Inc. | 07/01/2026SE |
| K261246 | SRGC-06EBF · Traditional | GC America, Inc. | 06/18/2026SE |
| K261093 | DiafilEBF · Traditional | DiaDent Group International | 06/02/2026SE |
| K261071 | DIAFIL Bulk FLOW (Economic Package);DIAFIL Bulk FLOW (Refill Package);DIAFIL Bulk FLOW…EBF · Traditional | DiaDent Group International | 05/19/2026SE |
| K260805 | Dual CoreEBF · Traditional | Vericom Co., Ltd. | 05/11/2026SE |
| K261357 | Grandio disc multicolorEBF · Traditional | Voco GmbH | 04/27/2026SE |
| K261356 | Dura-CrownEBF · Special | Hangzhou SHINING3D Dental Technology Co., Ltd. | 04/27/2026SE |
More from Hangzhou SHINING3D Dental Technology Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K863831 | Vivadent FilpinEBL · Traditional | 10/14/1986SE |
| K823409 | Heliosit-OrthodonticDYH · Traditional | 01/21/1983SE |
| K813015 | HeliosealEBC · Traditional | 12/02/1981SE |
| K802679 | SilanitEBG · Traditional | 12/17/1980SE |
| K802684 | HeliomatEAY · Traditional | 11/24/1980SE |
| K802683 | HeliositEBF · Traditional | 11/24/1980SE |
| K802682 | Contact SealEBC · Traditional | 11/24/1980SE |
| K802681 | HeliobondKLE · Traditional | 11/24/1980SE |
| K802685 | ReolitEJK · Traditional | 11/12/1980SE |
| K801227 | SilicapEMA · Traditional | 08/12/1980SE |
Questions and answers
When was Isopast-Ds cleared by the FDA?
Isopast-Ds (K802680) received a 510(k) decision of Substantially Equivalent on November 12, 1980, 15 days after the submission was received.
What is the product code of K802680?
The FDA product code is EBF – Material, Tooth Shade, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3690.