Alure Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Alure Medical, Inc. makes
Alure Medical, Inc. manufactures the REFINE LIFT SYSTEM and the REFINE SUPPORT SYSTEM (Model 100.0100), which are designed for spinal surgical applications to provide stabilization and support during 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
Refine Lift System Ref K083102
Regimes: 510(k) Registry: 510(k)Refine Support System, Model 100.0100 Ref K092538
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alure Medical, Inc. have in the registry?
The registry currently lists 2 devices for Alure Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alure Medical, Inc.'s devices?
Among its 2 most recently registered devices, Alure Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Alure Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Alure Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alure Medical, Inc. in the registry?
The most recently registered devices listed for Alure Medical, Inc. include REFINE LIFT SYSTEM and REFINE SUPPORT SYSTEM, MODEL 100.0100.