Registered with FDA
Factor, Ii, Inc.
Lakeside, AZ, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 2 510(k) clearances as applicant.
- Device types listed
- 2
- Brands and models
- 2
- 510(k) clearances
- 21983–2000
- Markets registered in
- 1United States
- Establishments
- 1United States
510(k) clearances per year, 1980–2026
Devices listed with FDA
What Factor, Ii, Inc. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Root-Form Endosseous ImplantDZE · Class 2 | Dental implants | Lister | MAGNABUTMENT | 2011 |
| All Precision AttachmentEGG · Class 1 | — | Lister | Magnacap | 2011 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
510(k) clearances
Clearances on which FDA names Factor, Ii, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 28 Jan 2000 | K984297 | MAGNA ABUTMENT | DZE Root-Form Endosseous Implant |
| 31 Aug 1983 | K831095 | ROYALE II | EBI Rebasing Repairing Relining Denture Resin |
Some of these clearances are listed with FDA today by another company: Technovent Limited (1).
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| FACTOR, II, INC.FDA reg. 2023623 | LAKESIDE, AZ, United States | Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 2023623). 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.