Cti Corp., Ltd.
Country not established
- Devices
- 1
What Cti Corp., Ltd. makes
Cti Corp., Ltd. manufactures laminaria, a cervical dilator used in obstetric procedures to gradually widen the cervix prior to labor or surgical intervention.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Laminaria Ref K955072
510(k) 510(k)
Frequently asked questions
How many devices does Cti Corp., Ltd. have in the registry?
The registry currently lists 1 device for Cti Corp., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cti Corp., Ltd.'s devices?
Among its 1 most recently registered device, Cti Corp., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cti Corp., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cti Corp., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cti Corp., Ltd. in the registry?
The most recently registered devices listed for Cti Corp., Ltd. include LAMINARIA.