Data / Medical devices / Indirect Bonding Tray / United States
FDA-registered makers of Indirect Bonding Tray in the United States: 19 establishments
19 establishments in the United States are registered with the FDA to make Indirect Bonding Tray (product code QJJ). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Indirect Bonding Tray
- Product code
- QJJ
- Country
- United States
Makers of Indirect Bonding Tray in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Alta Smiles, LLC | Fort Washington, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Align Technology, Inc. | San Jose, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Celebrace | Colleyville, TX, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ClearCorrect, LLC | Round Rock, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentsply Sirona Orthodontics Inc. | Sarasota, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dentsply Sirona Orthodontics Inc. | Richardson, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Five Star Orthodontic Laboratory & Supply, Inc. | Denton, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Johns Dental Laboratory | Terre Haute, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Klowen Braces Dba Klowen Orthodontics | Richardson, TX, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Keystone Industries | Myerstown, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Keystone Industries | Cherry Hill, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Keystone Industries - Gibbstown | Gibbstown, NJ, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orthoselect | American Fork, UT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ormco Corporation | Pomona, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ormco Corporation | Brea, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Specialty Appliances, LLC | Cumming, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sprintray Inc. | Los Angeles, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sprintray Inc. | Huntington Beach, CA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xplora USA LLC | Carrollton, TX, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.