Kavo Everest C-Temp
FDA 510(k) K063624 · Kavo America
510(k) numberK063624
Submission
- Device name
- Kavo Everest C-Temp
- Applicant
- Kavo America
Deer Field, IL, US - Received
- December 6, 2006
- Decision date
- February 8, 2007
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
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| K261261 | Dura-ArchEBG · Traditional | Hangzhou SHINING3D Dental Technology Co., Ltd. | 04/17/2026SE |
| K253380 | FLNT Base and FLNT TempEBG · Traditional | Liaoning Upcera Co., Ltd. | 03/02/2026SE |
| K251271 | TempFIT Temporary Crown and Bridge ResinEBG · Traditional | Rizhao Huge Biomaterials Company, Ltd. | 06/23/2025SE |
| K243370 | DentaTOOTHEBG · Traditional | Asiga Pty, Ltd. | 05/05/2025SE |
| K243621 | Evoblock, PerléonEBG · Traditional | Evoden Indústria Comércio Importação E Exportação | 04/22/2025SE |
| K243951 | TEMP MASTER, PMMA-based dental resinEBG · Traditional | Taiwan Dental Materials Co., Ltd. | 02/21/2025SE |
| K242559 | Digital TempEBG · Traditional | Sprintray, Inc. | 11/26/2024SE |
| K231859 | PrimmaArtEBG · Traditional | Dentscare Ltda | 11/26/2024SE |
| K240538 | Premium Teeth ResinEBG · Traditional | Formlabs Ohio, Inc. | 07/19/2024SE |
| K241226 | Fixtemp® C&B 4:1EBG · Special | Dreve Denatmid GmbH | 05/31/2024SE |
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| K051909 | DiagnodentNBL · Traditional | 10/21/2005SE |
| K030146 | Kavo Key Laser 1242 and Kavo Key Laser 1243+NVK · Traditional | 08/03/2005SE |
| K042394 | Diagnodent Perio Tip (Accessory)NBL · Traditional | 08/02/2005SE |
| K050744 | Kavo Ergocom/ErgocamLLZ · Traditional | 04/21/2005SE |
| K050019 | In Exam Intraoral Dental X-Ray SystemEHD · Traditional | 01/31/2005SE |
| K042872 | Rondoflex Plus 360KOJ · Special | 11/23/2004SE |
| K033221 | Kavo Everest Zh-BlankEIH · Special | 10/28/2003SE |
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Questions and answers
When was Kavo Everest C-Temp cleared by the FDA?
Kavo Everest C-Temp (K063624) received a 510(k) decision of Substantially Equivalent on February 8, 2007, 64 days after the submission was received.
What is the product code of K063624?
The FDA product code is EBG – Crown And Bridge, Temporary, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3770.