Not currently registered with FDA under this name
American Midwest
Mchenry, IL, United States. Named as applicant on 5 dental 510(k) clearances between 1980 and 1982. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51980–1982
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1980–2026
510(k) clearances
Clearances on which FDA names American Midwest as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 16 Jul 1982 | K821895 | AH-1 LIGHT-CURE DENTAL COMPOSITE RESTOR | EBF Resin Tooth Shade Material |
| 25 Jun 1982 | K821715 | AM-40 SYSTEM | EFB Dental Air-Powered Handpiece |
| 9 Apr 1982 | K820693 | MIDWEST LIGHT WAND | EBZ Ultraviolet Activator for Polymerization |
| 18 Aug 1981 | K811979 | ATT-1 DENTAL COMPOSITE RESTORATIVE SYS | EBF Resin Tooth Shade Material |
| 10 Apr 1980 | K800735 | U-STYLE ADAPTER | EGS Dental Contra- and Right-Angle Attachment Handpiece |
Some of these clearances are listed with FDA today by another company: Dentsply Sirona, Inc. (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.