Not currently registered with FDA under this name
J.L. Blosser, Inc.
Liberty, MO, United States. Named as applicant on 2 dental 510(k) clearances between 1993 and 2004. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 21993–2004
- Markets registered in
- 39 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1990–2026
Registered in 3 markets
Where regulators' registries name J.L. Blosser, Inc. 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 | J.L. Blosser, Inc. | 2 clearances | 1993–2004 | Below |
| Canada | Health Canada | Registration holder | J.L. BLOSSER INC. | 7 | 2006–2007 | Pure Global AI |
| South Korea | MFDS | Manufacturer | J.L.Blosser, IncJ.L.Blosser, Inc. | 2 | 2004–2005 | 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 J.L. Blosser, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 7 Apr 2004 | K040614 | BLUEWAND LED DENTAL CURING WAND SYSTEM | EBZ Ultraviolet Activator for Polymerization |
| 20 Oct 1993 | K933459 | RESIMENT WITH FLUORIDE | EMA Dental Cement |
Some of these clearances are listed with FDA today by another company: Sterngold (1).
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.