Medeering, Ltd.
Country not established
- Devices
- 1
What Medeering, Ltd. makes
Medeering, Ltd. manufactures silicone breast forms, designed as prosthetic devices for post-mastectomy patients or individuals requiring breast shaping.
The company’s silicone breast form falls under FDA Class I devices and is listed via a 510(k) pathway in the United States.
Catalogue
Trulife Silicone Breast Form Ref K831831
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medeering, Ltd. have in the registry?
The registry currently lists 1 device for Medeering, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medeering, Ltd.'s devices?
Among its 1 most recently registered device, Medeering, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Medeering, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medeering, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medeering, Ltd. in the registry?
The most recently registered devices listed for Medeering, Ltd. include TRULIFE SILICONE BREAST FORM.