Interphase Implants, Inc.
Country not established
- Devices
- 1
What Interphase Implants, Inc. makes
Interphase Implants, Inc. manufactures smooth staple implants, which are designed for surgical fixation in tissue. These devices are intended to provide secure closure or approximation of anatomical structures during procedures.
The company’s portfolio is regulated under Class II medical devices in the United States, with products listed via the FDA’s 510(k) clearance pathway. The manufacturer operates from the US.
Catalogue
Smooth Staple Implant Ref K900433
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Interphase Implants, Inc. have in the registry?
The registry currently lists 1 device for Interphase Implants, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interphase Implants, Inc.'s devices?
Among its 1 most recently registered device, Interphase Implants, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Interphase Implants, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Interphase Implants, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Interphase Implants, Inc. in the registry?
The most recently registered devices listed for Interphase Implants, Inc. include SMOOTH STAPLE IMPLANT.