Not currently registered with FDA under this name
Juell Dental
Ardmore, OK, United States. Named as applicant on 3 dental 510(k) clearances between 2011 and 2011. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 32011–2011
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Juell Dental as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 12 Sep 2011 | K111178 | JUELL SOFT CURE | EBI Rebasing Repairing Relining Denture Resin |
| 12 Sep 2011 | K111177 | JUELL HARD CURE | EBI Rebasing Repairing Relining Denture Resin |
| 29 Jul 2011 | K110548 | OSI O-BALL ABUTMENT HEAD IMPLANTS | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: Park Dental Research Corp (3).
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.