Not currently registered with FDA under this name
Cavitron Corp.
Mchenry, IL, United States. Named as applicant on 7 dental 510(k) clearances between 1976 and 1981. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 71976–1981
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1976–2026
510(k) clearances
Clearances on which FDA names Cavitron Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 28 Jul 1981 | K811582 | THE PLACER | EID Restorative and Impression Material Syringe |
| 19 Sep 1979 | K791585 | MODEL G-61 ULTRASONIC DENTAL UNIT | ELC Ultrasonic Scaler |
| 22 Jun 1978 | K780811 | DENTAL ABRASIVE DEVICE | EHL Abrasive Point |
| 14 Mar 1978 | K780377 | PINIDENTOFLEX DENTAL POLISHER | EHL Abrasive Point |
| 14 Mar 1978 | K780376 | MINIDENTOFLEX NEW POLISHING SYSTEM | EHL Abrasive Point |
| 12 Sep 1977 | K771658 | IDENTOFLEX | EHJ Abrasive Disk |
| 21 Oct 1976 | K760805 | ULTRASONIC DENTAL PROPHYLAXIS DEVICE | ELC Ultrasonic Scaler |
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.