Neen Design, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 1
What Neen Design, Ltd. makes
Neen Design, Ltd. manufactures the Periform Perineometric Probe (Model 8300), a device used for measuring perineal muscle strength and function, typically in clinical or research settings to assess pelvic floor integrity.
The Periform Perineometric Probe is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Periform Perineometric Probe, Model 8300 Ref K002617
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neen Design, Ltd. have in the registry?
The registry currently lists 1 device for Neen Design, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neen Design, Ltd.'s devices?
Among its 1 most recently registered device, Neen Design, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Neen Design, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neen Design, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Neen Design, Ltd. in the registry?
The most recently registered devices listed for Neen Design, Ltd. include PERIFORM PERINEOMETRIC PROBE, MODEL 8300.