LightForce Orthodontics
United Statesfrom the FDA registration address FDA FEI 3027460334
- Devices
- 34
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 34 devicesCompany details
- FDA FEI number
- 3027460334
- Address
- 400 Research Dr., Ste 125, Wilmington, MA, 01887
- Website
- lightforceortho.com/
- facebook.com/LightForceOrtho
- [email protected]
- Phone
- +18665063070
From the company website
LightForce delivers 3D printed patient-specific braces. Generated from a digital orthodontic treatment plan. Made for one. Born from light.
Frequently asked questions
How many devices does LightForce Orthodontics have in the registry?
The registry currently lists 34 devices for LightForce Orthodontics. Devices recorded under merged duplicate company entries are counted once.
Which registries list LightForce Orthodontics's devices?
Among its 34 most recently registered devices, LightForce Orthodontics has devices listed in FDA 510(k) (3 devices) and FDA GUDID (31 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do LightForce Orthodontics's devices fall under?
Among its 34 most recently registered devices, the classes recorded for LightForce Orthodontics's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from LightForce Orthodontics in the registry?
The most recently registered devices listed for LightForce Orthodontics include FlexBracket 09.01.25.PCA.FB.UL1.022, FlexBracket 09.01.25.PCA.FB.UL3.022, FlexBracket 09.01.25.PCA.FB.UL2.022 and FlexBracket 09.01.25.PCA.FB.UL4.022.