Serica Technologies, Inc.
Country not established
- Devices
- 1
What Serica Technologies, Inc. makes
Serica Technologies, Inc. manufactures surgical mesh products, including the SERISCAFFOLD Surgical Mesh, designed for use in hernia repair and related reconstructive procedures.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The manufacturer is based in the United States.
Catalogue
Seriscaffold Surgical Mesh Ref K080442
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Serica Technologies, Inc. have in the registry?
The registry currently lists 1 device for Serica Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Serica Technologies, Inc.'s devices?
Among its 1 most recently registered device, Serica Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Serica Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Serica Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Serica Technologies, Inc. in the registry?
The most recently registered devices listed for Serica Technologies, Inc. include SERISCAFFOLD SURGICAL MESH.