Stuart-Lee, Inc.
Country not established
- Devices
- 1
What Stuart-Lee, Inc. makes
Stuart-Lee, Inc. manufactures the Stuart Lee Clip, a Class I medical device designed for securing or stabilizing components in surgical or procedural settings.
The device is regulated under the FDA’s 510(k) pathway as a Class I product and is listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Stuart Lee Clip Ref K881741
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stuart-Lee, Inc. have in the registry?
The registry currently lists 1 device for Stuart-Lee, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stuart-Lee, Inc.'s devices?
Among its 1 most recently registered device, Stuart-Lee, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Stuart-Lee, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Stuart-Lee, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Stuart-Lee, Inc. in the registry?
The most recently registered devices listed for Stuart-Lee, Inc. include STUART LEE CLIP.