Data / Medical devices / Canada / Dental Wings Inc.
Dental Wings Inc.: FDA-registered device maker in Montreal Quebec, Canada, 1 510(k) clearance
Dental Wings Inc. is registered with the FDA (registration 3006945044) in Montreal Quebec, Canada. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 26, 2024. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3006945044
- Address
- 160 Rue Saint-Viateur E, Montreal Quebec, Canada, H2T 1A8
- Owner or operator
- INSTITUT STRAUMANN AG (9005052)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- January 24, 2008
- Registered through
- 2027
- Brand names listed
- AS200E, AS260, DI-1, DWOS, S300W, SIRIOS, ST 300E, ST200E and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dental Abutment Design Software For Dental Laboratory | PNP | 2 | Manufacturer | accessdata.fda.gov |
| System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations | NOF | 2 | Contract manufacturer, 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 |
|---|---|---|---|---|---|---|
| December 26, 2024 | K233252 | Straumann CARES Visual and Nova Dental CAD | PNP | Substantially Equivalent | Institut Straumann AG | accessdata.fda.gov |
Compare with other makers
- All makers of Dental Abutment Design Software For Dental Laboratory
- All makers of System, Optical Impression, Computer Assisted Design And Manufacturing (Cad/Cam) Of Dental Restorations
Updated December 26, 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.