Data / Medical devices / Canada / Safari Dental, Inc.
Safari Dental, Inc.: FDA-registered device maker in BOISBRIAND Quebec, Canada, 1 510(k) clearance
Safari Dental, Inc. is registered with the FDA (registration 9681829) in BOISBRIAND Quebec, Canada. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 22, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9681829
- FEI number
- 1000550533
- Address
- 94D Enterprises Boul., BOISBRIAND Quebec, Canada, J7G 2T3
- Owner or operator
- SAFARI DENTAL, INC. (9027483)
- Roles
- Manufacturer
- First device listed
- August 16, 1996
- Registered through
- 2026
- Brand names listed
- Operative Dental Unit, REFLECTED LIGHT, SAFARI DENTAL CHAIR, SAFARI DR'S STOOL
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chair, Examination And Treatment | FRK | 1 | Manufacturer | accessdata.fda.gov |
| Chair, With Casters | INM | 1 | Manufacturer | accessdata.fda.gov |
| Light, Operating, Dental | EAZ | 1 | Manufacturer | accessdata.fda.gov |
| Unit, Operative Dental | EIA | 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 |
|---|---|---|---|---|---|---|
| October 22, 2010 | K100212 | DENTACENTER/EXPEDITION, MODEL SAF-430 | EIA | Substantially Equivalent | Safari Dental, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Chair, With Casters
- All makers of Chair, Examination And Treatment
- All makers of Light, Operating, Dental
- All makers of Unit, Operative Dental
Updated October 22, 2010. 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.