Not currently registered with FDA under this name
Bosworth Co.
Skokie, IL, United States. Named as applicant on 4 dental 510(k) clearances between 1981 and 1999. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 41981–1999
- Markets registered in
- 22 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1980–2026
Registered in 2 markets
Where regulators' registries name Bosworth 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 | Bosworth Co. | 4 clearances | 1981–1999 | Below |
| Taiwan | TFDA | Manufacturer | BOSWORTH COMPANY | 2 | 2010–2021 | 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 Bosworth Co. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 7 Oct 1999 | K991687 | MODIFICATION TO LINER II: SOFT RELINE LIQUID | EBI Rebasing Repairing Relining Denture Resin |
| 26 Jul 1999 | K991902 | LC PIT & FISSURE SEALANT | EBC Pit and Fissure Sealant and Conditioner |
| 28 Aug 1995 | K953119 | BOSWORTH RESIN II | EBI Rebasing Repairing Relining Denture Resin |
| 2 Feb 1981 | K810094 | DENTURE RUBBER BASE MATERIAL | EBI Rebasing Repairing Relining Denture Resin |
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.