Not currently registered with FDA under this name
Sybron Corp.
Washington, DC, United States. Named as applicant on 13 dental 510(k) clearances between 1977 and 1986. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 131977–1986
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1976–2026
510(k) clearances
Clearances on which FDA names Sybron Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 23 Jun 1986 | K862284 | SEALITE | EBC Pit and Fissure Sealant and Conditioner |
| 30 Jan 1986 | K854855 | PROOF ALGINATE IMPRESSION MATERIAL | ELW Impression Material |
| 13 Jul 1984 | K841910 | KERR SEALAPEX ROOT CANAL SEALER | EJK Calcium Hydroxide Cavity Liner |
| 21 May 1984 | K840407 | KERR RESIN BONDED BRIDGE CEMENT | EMA Dental Cement |
| 26 Jan 1983 | K823795 | EVERBOND GLASS IONOMER CEMENT | EMA Dental Cement |
| 13 Oct 1982 | K822869 | COMMAND BONDING RESIN/GLAZE/OPAQUER | EBD Resin Filling Material Coating |
| 2 Mar 1982 | K820182 | SYBRON/KERR COMMAND | EBF Resin Tooth Shade Material |
| 24 Feb 1982 | K820183 | SYBRON/KERR MIRROR 3 | ELW Impression Material |
| 24 Feb 1982 | K820181 | SYBRON/KERR CONTOUR | EJJ Amalgam Alloy |
| 4 Aug 1980 | K801529 | KERR CORE COMPOSITE | EBF Resin Tooth Shade Material |
| 28 Jul 1980 | K801530 | COREFORM MOLDS | DZN Dental Hand Instruments |
| 17 Mar 1980 | K800276 | RITTER MODEL H COMPANION STOOL | KLC Dental Chair with Operative Unit |
| 2 Dec 1977 | K772164 | PANORAMIC X-RAY SYSTEM MODEL A | EHD Extraoral with Timer X-Ray Unit |
Some of these clearances are listed with FDA today by another company: Sybron Dental Specialties (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.