Sites Medical, LLC
United Statesfrom the FDA registration address FDA FEI 3009923578
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Sites Medical, LLC makes
Sites Medical, LLC manufactures OsteoSync™ Ti Dental Mesh, a titanium mesh designed for use in dental and maxillofacial reconstruction procedures to support bone regeneration and structural integrity.
The company’s portfolio is regulated under FDA Class II devices, with authorisation records maintained through the 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
OsteoSync™ Ti Dental Mesh Ref K202918
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009923578
- Address
- 4707 E Park 30 Drive, Columbia City, IN, 46725
Frequently asked questions
How many devices does Sites Medical, LLC have in the registry?
The registry currently lists 1 device for Sites Medical, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sites Medical, LLC's devices?
Among its 1 most recently registered device, Sites Medical, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Sites Medical, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sites Medical, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sites Medical, LLC in the registry?
The most recently registered devices listed for Sites Medical, LLC include OsteoSync™ Ti Dental Mesh.