Mentor Medical Limited
United KingdomFDA applicant, unverified
- Devices
- 1
What Mentor Medical Limited makes
Mentor Medical Limited manufactures percutaneous dilatational tracheostomy kits, designed for creating surgical airways in patients requiring long-term respiratory support.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mentor Medical Limited have in the registry?
The registry currently lists 1 device for Mentor Medical Limited. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mentor Medical Limited's devices?
Among its 1 most recently registered device, Mentor Medical Limited has devices listed in FDA 510(k) (1 device).
What risk classes do Mentor Medical Limited's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mentor Medical Limited's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mentor Medical Limited in the registry?
The most recently registered devices listed for Mentor Medical Limited include PORTEX PERCUTANEOUS DILATATIONAL TRACHEOSTOMY KITS.