Mle, Inc.
Country not established
- Devices
- 1
What Mle, Inc. makes
Mle, Inc. manufactures suture fixation devices and mesh fixation devices, which are used in surgical procedures to secure tissues and implants within the body.
These products are classified as Class II medical devices under US regulations and are listed via the FDA’s 510(k) pathway. The company operates from the United States.
Catalogue
Suture Fixation Device; Mesh Fixation Device Ref K021834
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mle, Inc. have in the registry?
The registry currently lists 1 device for Mle, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mle, Inc.'s devices?
Among its 1 most recently registered device, Mle, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Mle, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Mle, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mle, Inc. in the registry?
The most recently registered devices listed for Mle, Inc. include SUTURE FIXATION DEVICE; MESH FIXATION DEVICE.