Not currently registered with FDA under this name
Sherwood Medical Co.
Mchenry, IL, United States. Named as applicant on 4 dental 510(k) clearances between 1979 and 1980. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 41979–1980
- Markets registered in
- 454 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1976–2026
Registered in 4 markets
Where regulators' registries name Sherwood Medical Co. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Sherwood Medical Co. | 4 clearances | 1979–1980 | Below |
| Taiwan | TFDA | Manufacturer | SHERWOOD MEDICAL COMPANY.SHERWOOD MEDICAL COMPANY · SHERWOOD MEDICAL CO · +1 | 44 | 1974–1997 | Pure Global AI |
| South Korea | MFDS | Manufacturer | SHERWOOD MEDICAL CO.Sherwood Medical Co. | 9 | 1999–1999 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | SHERWOOD MEDICAL COMPANY | 1 | — | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
510(k) clearances
Clearances on which FDA names Sherwood Medical Co. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 24 Nov 1980 | K802811 | MONOJECT ROOT CANAL FILLING MAT. NEEDLE | DZM Dental Needle |
| 1 Feb 1980 | K792541 | MONOJECT PLASTIC DENTAL INJ. SYRINGE | EJI Cartridge Syringe |
| 22 Oct 1979 | K791088 | MONOJECT PULP-CAPPING MATERIAL | EJK Calcium Hydroxide Cavity Liner |
| 17 Oct 1979 | K791326 | MONOJECT ENDOSSEOUS DENTAL IMPLANT TOOL | DZI Powered Bone Drill |
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.