Data / Medical devices / United States / Progressive Orthodontics USA
Progressive Orthodontics USA: FDA-registered device maker in Aliso Viejo, CA, United States, 1 510(k) clearance
Progressive Orthodontics USA is registered with the FDA (registration 3017545364) in Aliso Viejo, CA, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 11, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017545364
- Address
- 135 Columbia Ste 101, Aliso Viejo, CA, United States, 92656
- Owner or operator
- Progressive America Inc (10096078)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- June 18, 2026
- Registered through
- 2026
- Brand names listed
- Medit Orthodontic Suite
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Band, Material, Orthodontic | DYO | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Bracket, Metal, Orthodontic | EJF | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Orthodontic Software | PNN | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| System, Image Processing, Radiological | LLZ | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Wire, Orthodontic | DZC | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| October 11, 2024 | K241153 | Progressive Orthodontics App | PNN | Substantially Equivalent | Progressive Aligners, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Bracket, Metal, Orthodontic
- All makers of Orthodontic Software
- All makers of System, Image Processing, Radiological
- All makers of Band, Material, Orthodontic
- All makers of Wire, Orthodontic
Updated October 11, 2024. 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.