Safari Dental, Inc.
CanadaFDA applicant, unverified FDA FEI 1000550533
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Safari Dental, Inc. makes
Safari Dental, Inc. manufactures the Dentacenter/Expedition (Model SAF-430), a dental chair designed for clinical use in dental offices.
The company’s portfolio is regulated under FDA Class I devices and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Dentacenter/Expedition, Model Saf-430 Ref K100212
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000550533
- Address
- 94D ENTERPRISES BOUL., BOISBRIAND Quebec
Frequently asked questions
How many devices does Safari Dental, Inc. have in the registry?
The registry currently lists 1 device for Safari Dental, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Safari Dental, Inc.'s devices?
Among its 1 most recently registered device, Safari Dental, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Safari Dental, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Safari Dental, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Safari Dental, Inc. in the registry?
The most recently registered devices listed for Safari Dental, Inc. include DENTACENTER/EXPEDITION, MODEL SAF-430.