Archy Dental, Inc.
United Statesfrom the FDA registration address FDA FEI 3042655017
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Archy Dental, Inc. makes
Archy Dental, Inc. manufactures dental imaging systems designed for intraoral and extraoral radiographic procedures, including digital sensors and associated software for capturing and processing dental radiographs.
The company’s portfolio is regulated under FDA Class II devices and includes submissions via the 510(k) pathway. Products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Archy Dental Imaging Ref K251880
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3042655017
- Address
- 3031 Tisch Way, San Jose, CA, 95128
Frequently asked questions
How many devices does Archy Dental, Inc. have in the registry?
The registry currently lists 1 device for Archy Dental, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Archy Dental, Inc.'s devices?
Among its 1 most recently registered device, Archy Dental, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Archy Dental, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Archy Dental, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Archy Dental, Inc. in the registry?
The most recently registered devices listed for Archy Dental, Inc. include Archy Dental Imaging.