Lntegra Lifesciences
Country not established
- Devices
- 1
What Lntegra Lifesciences makes
Lintea LifeSciences manufactures a polydioxanone-based surgical scaffold designed for tissue integration and wound healing applications, supporting soft tissue reconstruction and repair procedures.
The company’s product portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Polydioxanone Surgical Scaffold Ref K181094
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lntegra Lifesciences have in the registry?
The registry currently lists 1 device for Lntegra Lifesciences. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lntegra Lifesciences's devices?
Among its 1 most recently registered device, Lntegra Lifesciences has devices listed in FDA 510(k) (1 device).
What risk classes do Lntegra Lifesciences's devices fall under?
Among its 1 most recently registered device, the classes recorded for Lntegra Lifesciences's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lntegra Lifesciences in the registry?
The most recently registered devices listed for Lntegra Lifesciences include Polydioxanone Surgical Scaffold.