Not currently registered with FDA under this name
Kavo America
Deer Field, IL, United States. Named as applicant on 17 dental 510(k) clearances between 1994 and 2007. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 171994–2007
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Kavo America as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 8 Feb 2007 | K063624 | KAVO EVEREST C-TEMP | EBG Resin Temporary Crown and Bridge |
| 21 Oct 2005 | K051909 | DIAGNODENT | NBL Light-Induced Fluorescence Caries Detector |
| 2 Aug 2005 | K042394 | DIAGNODENT PERIO TIP (ACCESSORY) | NBL Light-Induced Fluorescence Caries Detector |
| 31 Jan 2005 | K050019 | IN EXAM INTRAORAL DENTAL X-RAY SYSTEM | EHD Extraoral with Timer X-Ray Unit |
| 23 Nov 2004 | K042872 | RONDOFLEX PLUS 360 | KOJ Airbrush |
| 28 Oct 2003 | K033221 | KAVO EVEREST ZH-BLANK | EIH Porcelain Powder |
| 24 Jul 2003 | K032081 | KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60 | EIH Porcelain Powder |
| 9 Jul 2003 | K031868 | PROPHYPEARLS | EFB Dental Air-Powered Handpiece |
| 2 May 2003 | K030607 | KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES | EIH Porcelain Powder |
| 12 Mar 2003 | K024214 | KAVO EVEREST TITANBLANK | EJH Base Metal Alloy |
| 26 Jun 2002 | K012308 | KAVO QUATTROCARE | EFB Dental Air-Powered Handpiece |
| 14 Jan 2002 | K013500 | KAVO POLYLUX II | EBZ Ultraviolet Activator for Polymerization |
| 28 Nov 2000 | K002708 | KAVO CORUND HANDPIECE 2013 | KOJ Airbrush |
| 22 Feb 2000 | DEN990002 | KAVO DIAGNODENT | NBL Light-Induced Fluorescence Caries Detector |
| 19 Dec 1997 | K973876 | PROPHYFLEX 2, MODEL 2012 | EFB Dental Air-Powered Handpiece |
| 29 Dec 1994 | K940950 | KAVO SYSTEMATICA 1060 | KLC Dental Chair with Operative Unit |
| 16 May 1994 | K934783 | KAVO INTRASEPT 905 | EIA Operative Dental Unit |
Some of these clearances are listed with FDA today by another company: KaVo Dental GmbH (4).
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.