Manufacturer registered with FDA
World Class Technology Corporation
McMinnville, OR, United States. Lists 11 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 11
- Brands and models
- 25
- 510(k) clearances
- 12019–2019
- Markets registered in
- 121,120 registrations outside the US
- Establishments
- 1United States
510(k) clearances per year, 2007–2026
Registered in 12 markets
Where regulators' registries name World Class Technology Corporation 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 | World Class Technology Corporation | 1 clearances | 2019–2019 | Below |
| European Union | EUDAMED | Manufacturer | World Class Technology Corporation | 625 | — | Pure Global AI |
| Thailand | Thai FDA | Manufacturer | WORLD CLASS TECHNOLOGY CORPORATION | 230 | — | Pure Global AI |
| Canada | Health Canada | Registration holder | WORLD CLASS TECHNOLOGY CORPORATION | 197 | 2009–2026 | Pure Global AI |
| Costa Rica | Ministerio de Salud | Manufacturer | WORLD CLASS TECHNOLOGY CORPORATION | 23 | — | Pure Global AI |
| South Korea | MFDS | Manufacturer | World Class Technology Corporation | 15 | 2007–2015 | Pure Global AI |
| Peru | DIGEMID | Manufacturer | WORLD CLASS TECHNOLOGY CORPORATION | 10 | 2010–2025 | Pure Global AI |
| United Kingdom | MHRA | Manufacturer | World Class Technology Corporation | 7 | — | Pure Global AI |
| Serbia | ALIMS | Manufacturer | World Class Technology Corporation | 6 | 2024–2024 | Pure Global AI |
| Israel | AMAR | Manufacturer | World Class TechnologyWorld Class Technology Corporation | 3 | — | Pure Global AI |
| Taiwan | TFDA | Manufacturer | WORLD CLASS TECHNOLOGYWORLD CLASS TECHNOLOGY CORPORATION · World Class Technology Corporation | 3 | 2007–2022 | Pure Global AI |
| Vietnam | IMDA | Registration holder | WORLD CLASS TECHNOLOGY CORPORATION | 1 | — | 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 World Class Technology Corporation currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Orthodontic Material BandDYO · Class 1 | Orthodontic wires & bands | Maker | DurabandFierroorthodontic band | 2009 |
| Orthodontic WireDZC · Class 1 | Orthodontic wires & bands | Maker | orthodontic wire | 2009 |
| Orthodontic TubeDZD · Class 1 | Orthodontic wires & bands | Maker | BioMiniH4/Pitts21 | 2009 |
| Dental Hand InstrumentsDZN · Class 1 | Dental hand instruments | Maker | Archwire Seating InstrumentDebonding InstrumentDirector ToolElastic Placement ToolH4/Pitts21 ToolPositioning ToolQuick Turn Tool | 2022 |
| Dental Diamond InstrumentDZP · Class 1 | Dental burs & diamonds | Lister | Diamond DiscInterproximal Reduction (IPR) | 2022 |
| Resin Tooth Shade MaterialEBF · Class 2 | Dental composites | Lister | Aspire | 2020 |
| Orthodontic Elastic BandECI · Class 1 | Orthodontic wires & bands | Maker | orthodontic elastic band- multiple | 2009 |
| Orthodontic Wire ClampECN · Class 1 | — | Maker | Premium Crimpable Attachment/Micro Stop | 2022 |
| Orthodontic SpringECO · Class 1 | Orthodontic wires & bands | Maker | OC ORTHODONTICS SPRINGS | 2020 |
| Orthodontic Metal BracketEJF · Class 1 | Orthodontic brackets | Maker | APII Class 2 CorrectorBioMIMH4Pitts21Pitts21 PRO | 2004 |
| Orthodontic Ceramic BracketNJM · Class 2 | Orthodontic brackets | Maker | Clear21 | 2020 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
World Class Technology Corporation lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Prime Dental Manufacturing, Inc. (1).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 30 May 2000 | K001108 | PRIME-DENT VISIBLE LIGHT CURE COMPOSITE RESTORATIVE MATERIAL | Prime Dental Manufacturing, Inc. | EBF Resin Tooth Shade Material |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| WORLD CLASS TECHNOLOGY CORPORATIONFDA reg. 3003971538 | MCMINNVILLE, OR, United States | Manufacturer, Repacker / relabeler |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 9062858). 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.