Not currently registered with FDA under this name
Midwest Dental Products Corp.
Des Plaines, IL, United States. Named as applicant on 5 dental 510(k) clearances between 1996 and 1998. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51996–1998
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Midwest Dental Products Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 11 Mar 1998 | K973800 | 23:1 REDUCTION ANGLE | EGS Dental Contra- and Right-Angle Attachment Handpiece |
| 11 Sep 1997 | K964755 | MICROJET CAVITY PREPARATION SYSTEM | KOJ Airbrush |
| 18 Oct 1996 | K962877 | MIDWEST 300 SE | EFB Dental Air-Powered Handpiece |
| 11 Oct 1996 | K963050 | TRADITION P, PUSH BUTTON HANDPIECE | EFB Dental Air-Powered Handpiece |
| 5 Mar 1996 | K955655 | MIDWEST ONE | EFB Dental Air-Powered Handpiece |
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.