Ortho-Cycle Co.
United Statesfrom the FDA registration address FDA FEI 1052235
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Refurbished Orthodontic Appliances Ref K913913
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1052235
- Address
- 2026 Scott St, HOLLYWOOD, FL, 33020
Frequently asked questions
How many devices does Ortho-Cycle Co. have in the registry?
The registry currently lists 1 device for Ortho-Cycle Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ortho-Cycle Co.'s devices?
Among its 1 most recently registered device, Ortho-Cycle Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Ortho-Cycle Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ortho-Cycle Co.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ortho-Cycle Co. in the registry?
The most recently registered devices listed for Ortho-Cycle Co. include REFURBISHED ORTHODONTIC APPLIANCES.