Not currently registered with FDA under this name
Spintech, Inc.
Washington, DC, United States. Named as applicant on 4 dental 510(k) clearances between 1996 and 2003. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 41996–2003
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Spintech, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 2 Sep 2003 | K023722 | SAFETYWAND DISPOSABLE HANDPIECE | EJI Cartridge Syringe |
| 11 May 2000 | K992819 | WAND PLUS | EJI Cartridge Syringe |
| 5 Jul 1996 | K961648 | THE WAND | EJI Cartridge Syringe |
| 8 Feb 1996 | K955654 | SHORTSTOP DISPOSABLE PROPHY ANGLE | EFB Dental Air-Powered Handpiece |
Some of these clearances are listed with FDA today by another company: Milestone Scientific, Inc. (2).
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.