Not currently registered with FDA under this name
Lares Manufacturing Co., Inc.
Mchenry, IL, United States. Named as applicant on 6 dental 510(k) clearances between 1978 and 1983. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 61978–1983
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1976–2026
510(k) clearances
Clearances on which FDA names Lares Manufacturing Co., Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 14 Nov 1983 | K831351 | PERMALUX VISIBLE CURE COMPOSITE RESTOR | EBF Resin Tooth Shade Material |
| 16 Dec 1980 | K801535 | LARES HANDPIECE OIL | EFB Dental Air-Powered Handpiece |
| 21 Jul 1980 | K801592 | FIBER OPTIC HOSE | EAY Dental Fiber Optic Light |
| 21 Jul 1980 | K801591 | FIBER OPTIC ILLUMINATOR | EAY Dental Fiber Optic Light |
| 14 Jul 1980 | K801534 | LARES AIR PRESSURE GAUGE | EIA Operative Dental Unit |
| 20 Jan 1978 | K780038 | DENTAL HANDPIECE | 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.