Cera R Plus Alloy
FDA 510(k) K032319 · Dentsply International
510(k) numberK032319
Submission
- Device name
- Cera R Plus Alloy
- Applicant
- Dentsply International
York, PA, US - Received
- July 28, 2003
- Decision date
- September 30, 2003
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Other 510(k)s with product code EJT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K052463 | Prometal HN86EJT · Traditional | Prometal Technologies | 10/14/2005SE |
| K041378 | Bio 60EJT · Traditional | Kodent, Inc. | 08/02/2004SE |
| K040672 | Porta ReflexEJT · Traditional | Wieland Dental + Technik GmbH & Co. KG | 05/27/2004SE |
| K040524 | Porta Solder 1090 WEJT · Traditional | Wieland Dental + Technik GmbH & Co. KG | 05/20/2004SE |
| K040043 | NDX-40 AlloyEJT · Traditional | Heraeus Kulzer, Inc. | 03/03/2004SE |
| K034049 | Herador Ec, PF, C, H, NH, G, GG and MP; Heraloy U and G; Herabond N; Albabond C, B and…EJT · Traditional | Heraeus Kulzer,GmbH | 03/01/2004SE |
| K033279 | Gold Dental Casting AlloysEJT · Traditional | Bego U.S.A. | 01/15/2004SE |
| K033446 | APEX93, APEX87, APEX84, APEX85, APEX77, E-Sarang 88 and E-Sarang 82EJT · Traditional | We Dong Myung Dental Industrial Co., Ltd. | 11/13/2003SE |
| K033435 | E-Sarang 86, DM78, DM55EJT · Traditional | We Dong Myung Dental Industrial Co., Ltd. | 11/12/2003SE |
| K032320 | Appollo 3 AlloyEJT · Traditional | Dentsply International | 10/01/2003SE |
More from Dentsply International
| 510(k) | Device | Decision |
|---|---|---|
| K160207 | ATLANTIS ISUS Implant SuprastructuresNHA · Traditional | 09/21/2016SE |
| K160232 | Disposable Barrier Sleeves and CoversPEM · Traditional | 06/07/2016SE |
| K151439 | Atlantis IsusNHA · Traditional | 02/19/2016SE |
| K152247 | ATLANTIS CrownEIH · Traditional | 01/29/2016SE |
| K151039 | ATLANTIS Abutment for NobelActive 3.0NHA · Traditional | 01/14/2016SE |
| K151619 | Prime&Bond Elect Universal Dental AdhesiveKLE · Traditional | 10/30/2015SE |
| K150535 | Cavitron Touch Ultrasonic Scaling SystemELC · Traditional | 06/16/2015SE |
| K142178 | Proroot Mta White, Proroot Mta GrayKIF · Traditional | 02/26/2015SE |
| K131907 | Raypex 6LQY · Traditional | 01/31/2014SE |
| K131644 | Ankylos Syncone Abutment 5(DEGREE)NHA · Traditional | 01/22/2014SE |
Questions and answers
When was Cera R Plus Alloy cleared by the FDA?
Cera R Plus Alloy (K032319) received a 510(k) decision of Substantially Equivalent on September 30, 2003, 64 days after the submission was received.
What is the product code of K032319?
The FDA product code is EJT – Alloy, Gold-Based Noble Metal, a Class II (moderate risk) device regulated under 21 CFR 872.3060.