Salumedica, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Salumedica, LLC makes
Salumedica, LLC manufactures nerve protection devices, including the Salumedica Nerve Cuff and the Salutunnel Nerve Protector (models ED-20329, ED-20330, ED-20331), designed to safeguard peripheral nerves during surgical procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Salumedica Nerve Cuff Ref K002098
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Salumedica, LLC have in the registry?
The registry currently lists 2 devices for Salumedica, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Salumedica, LLC's devices?
Among its 2 most recently registered devices, Salumedica, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Salumedica, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Salumedica, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Salumedica, LLC in the registry?
The most recently registered devices listed for Salumedica, LLC include SALUMEDICA NERVE CUFF and SALUTUNNEL NERVE PROTECTOR, MODEL ED-20329, ED-20330, ED-20331.