Sterinc
Country not established
- Devices
- 1
What Sterinc makes
Sterinc manufactures vaginal ports, including both sterile and non-sterile variants designed for medical procedures. These devices serve as access points for instruments or fluids during gynecological interventions.
The company’s products fall under FDA Class II regulation and are listed via the 510(k) pathway. Sterinc is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sterinc have in the registry?
The registry currently lists 1 device for Sterinc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterinc's devices?
Among its 1 most recently registered device, Sterinc has devices listed in FDA 510(k) (1 device).
What risk classes do Sterinc's devices fall under?
Among its 1 most recently registered device, the classes recorded for Sterinc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sterinc in the registry?
The most recently registered devices listed for Sterinc include VAGINAL PORT, NON-STERILE / 600065, VAGINAL PORT, STERILE / 600073.