Iconlab, Inc.
Country not established
- Devices
- 1
What Iconlab, Inc. makes
Iconlab, Inc. manufactures Reperen Surgical Mesh, a product designed for surgical applications requiring tissue reinforcement or repair.
The company’s portfolio is regulated under FDA’s Class II device classification, with Reperen Surgical Mesh authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Reperen Surgical Mesh Ref K170134
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iconlab, Inc. have in the registry?
The registry currently lists 1 device for Iconlab, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iconlab, Inc.'s devices?
Among its 1 most recently registered device, Iconlab, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Iconlab, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Iconlab, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iconlab, Inc. in the registry?
The most recently registered devices listed for Iconlab, Inc. include Reperen Surgical Mesh.