Data / Medical devices / United States / World Class Technology Corporation
World Class Technology Corporation: FDA-registered device maker in Mcminnville, OR, United States, 2 510(k) clearances
World Class Technology Corporation is registered with the FDA (registration 3003971538) in Mcminnville, OR, United States. It lists 11 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 12, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003971538
- Address
- 1300 NE Alpha Dr, Mcminnville, OR, United States, 97128
- Owner or operator
- World Class Technology Corporation (9062858)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- April 16, 2004
- Registered through
- 2026
- Brand names listed
- APII Class 2 Corrector, Archwire Seating Instrument, Aspire, BioMIM, BioMini, Clear21, Debonding Instrument, Diamond Disc and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Band, Elastic, Orthodontic | ECI | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Band, Material, Orthodontic | DYO | 1 | Manufacturer | accessdata.fda.gov |
| Bracket, Ceramic, Orthodontic | NJM | 2 | Manufacturer | accessdata.fda.gov |
| Bracket, Metal, Orthodontic | EJF | 1 | Manufacturer | accessdata.fda.gov |
| Clamp, Wire, Orthodontic | ECN | 1 | Manufacturer | accessdata.fda.gov |
| Instrument, Diamond, Dental | DZP | 1 | Repackager or relabeler | accessdata.fda.gov |
| Instruments, Dental Hand | DZN | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Material, Tooth Shade, Resin | EBF | 2 | Repackager or relabeler | accessdata.fda.gov |
| Spring, Orthodontic | ECO | 1 | Manufacturer | accessdata.fda.gov |
| Tube, Orthodontic | DZD | 1 | Manufacturer | accessdata.fda.gov |
| Wire, Orthodontic | DZC | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 12, 2019 | K192202 | Clear21 | NJM | Substantially Equivalent | World Class Technology Corporation | accessdata.fda.gov |
| May 30, 2000 | K001108 | PRIME-DENT VISIBLE LIGHT CURE COMPOSITE RESTORATIVE MATERIAL | EBF | Substantially Equivalent | Prime Dental Manufacturing, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Instrument, Diamond, Dental
- All makers of Wire, Orthodontic
- All makers of Instruments, Dental Hand
- All makers of Bracket, Metal, Orthodontic
- All makers of Tube, Orthodontic
- All makers of Clamp, Wire, Orthodontic
Updated November 12, 2019. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.