Orquest, Inc.
Country not established
- Devices
- 1
What Orquest, Inc. makes
Orquest, Inc. manufactures HEALOS, a bone graft material designed for orthopedic and spinal surgical applications. The product is intended to support bone regeneration and integration in procedures requiring structural support or augmentation.
HEALOS is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Healos Bone Graft Material Ref K012751
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orquest, Inc. have in the registry?
The registry currently lists 1 device for Orquest, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orquest, Inc.'s devices?
Among its 1 most recently registered device, Orquest, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Orquest, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orquest, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orquest, Inc. in the registry?
The most recently registered devices listed for Orquest, Inc. include HEALOS BONE GRAFT MATERIAL.