Not currently registered with FDA under this name
Megagen Co., Ltd.
Brea, CA, United States. Named as applicant on 9 dental 510(k) clearances between 2005 and 2011. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 92005–2011
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Megagen Co., Ltd. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 22 Nov 2011 | K110955 | ANYRIDGE INTERNAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 3 Feb 2011 | K101890 | BALL ABUTMENT SYSTEM | NHA Endosseous Dental Implant Abutment |
| 11 Apr 2008 | K073058 | RESCUE INTERNAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 18 May 2007 | K070562 | EZ PLUS IMPLANT SYSTEM | NHA Endosseous Dental Implant Abutment |
| 2 Apr 2007 | K063216 | RESCUE INTERNAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 19 Apr 2006 | K053353 | RESCUE IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 13 Apr 2006 | K053354 | INTERMEZZO PLUS FIXTURE | DZE Root-Form Endosseous Implant |
| 10 Jan 2006 | K052369 | EXFEEL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 2 Sep 2005 | K051018 | INTERMEZZO IMPLANT SYSTEMS | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: Megagen Implant Co., Ltd. (8).
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.