Not currently registered with FDA under this name
Ronvig A/S
Daugaard, Denmark. Named as applicant on 2 dental 510(k) clearances between 2001 and 2003. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 22001–2003
- Markets registered in
- 24 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 2000–2026
Registered in 2 markets
Where regulators' registries name Ronvig A/S as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Ronvig A/S | 2 clearances | 2001–2003 | Below |
| South Korea | MFDS | Manufacturer | Ronvig A/S | 4 | 2001–2001 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
510(k) clearances
Clearances on which FDA names Ronvig A/S as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 22 Dec 2003 | K032925 | B&R DEVICE | EGS Dental Contra- and Right-Angle Attachment Handpiece |
| 10 May 2001 | K010816 | DENTO-PREP PARTICLE MICROBLASTER | KOJ Airbrush |
Some of these clearances are listed with FDA today by another company: Ronvig Dental Mfg. A/S (1).
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.