Not currently registered with FDA under this name
Riskontrol
Santa Fe, NM, United States. Named as applicant on 1 dental 510(k) clearance between 1993 and 1993. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 11993–1993
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Riskontrol as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 5 Apr 1993 | K923876 | RISKONTROL SINGLE USE | ECB Air and/or Water Syringe Unit |
Some of these clearances are listed with FDA today by another company: Satelec - Acteon Group (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.