Manufacturer registered with FDA
Bird-X, Inc.
Elmhurst, IL, United States. Lists 4 dental device types with FDA across 1 registered establishment.
- Device types listed
- 4
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 32 registrations outside the US
- Establishments
- 1United States
Registered in 3 markets
Where regulators' registries name Bird-X, 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 | Manufacturer | Bird-X, Inc. | 4 device types | — | Below |
| Canada | Health Canada | Registration holder | YATES-MOTLOID | 1 | 2016–2016 | Pure Global AI |
| South Korea | MFDS | Manufacturer | Yates-Motloid, Inc | 1 | 2012–2012 | 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
Devices listed with FDA
What Bird-X, 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 |
|---|---|---|---|---|
| Resin Temporary Crown and BridgeEBG · Class 2 | Temporary crown & bridge materials | Maker | Coldpac Tooth Acrylic | 2008 |
| Rebasing Repairing Relining Denture ResinEBI · Class 2 | Denture resins & teeth | Maker | Coldpac Denture Acrylic | 2014 |
| Intraoral Dental WaxEGD · Class 1 | — | Lister | All Season, Red Refined, Rijform, Set Rite | 2015 |
| Dental Wax CarverEIK · Class 1 | Dental hand instruments | Lister | Waxiron | 2012 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| YATES-MOTLOIDFDA reg. 1416675 | Elmhurst, IL, United States | Manufacturer, Repacker / relabeler |
Other names on FDA records
Yates-Motloid, Inc
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9914036). 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.