Therics, LLC
United StatesFDA applicant, unverified
- Devices
- 4
What Therics, LLC makes
Therics, LLC manufactures bone graft substitutes and void fillers for orthopedic and spinal applications, including putty formulations and block implants designed to support bone healing and structural integrity.
These products are classified as Class II medical devices under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Therilink Bone Void Filler Ref K040134
Regimes: 510(k) Registry: 510(k)Theriridge Block, Bone Graft Substitute Ref K023998
Regimes: 510(k) Registry: 510(k)Therifil Bone Filler Ref K031040
Regimes: 510(k) Registry: 510(k)Therigraft Tcp Putty Bone Void Filler Ref K053228
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Therics, LLC have in the registry?
The registry currently lists 4 devices for Therics, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Therics, LLC's devices?
Among its 4 most recently registered devices, Therics, LLC has devices listed in FDA 510(k) (4 devices).
What risk classes do Therics, LLC's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Therics, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Therics, LLC in the registry?
The most recently registered devices listed for Therics, LLC include THERILINK BONE VOID FILLER, THERIRIDGE BLOCK, BONE GRAFT SUBSTITUTE, THERIFIL BONE FILLER and THERIGRAFT TCP PUTTY BONE VOID FILLER.