Medisurg, Ltd.
Country not established
- Devices
- 4
What Medisurg, Ltd. makes
Medisurg, Ltd. manufactures surgical blades designed for ophthalmic procedures, including glaucoma surgery, peripheral iridotomy, and dental applications. The Fugo Blade series is intended for precise tissue incision in these specialized medical fields.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
The Fugo Blade For Glaucoma Ref K041019
Regimes: 510(k) Registry: 510(k)The Fugo Blade Ref K001498
Regimes: 510(k) Registry: 510(k)The Fugo Blade For Dentistry Ref K063468
Regimes: 510(k) Registry: 510(k)Fugo Blade For Peripheral Iridotomy, Model M300 Ref K050933
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medisurg, Ltd. have in the registry?
The registry currently lists 4 devices for Medisurg, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medisurg, Ltd.'s devices?
Among its 4 most recently registered devices, Medisurg, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medisurg, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medisurg, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medisurg, Ltd. in the registry?
The most recently registered devices listed for Medisurg, Ltd. include THE FUGO BLADE FOR GLAUCOMA, THE FUGO BLADE, THE FUGO BLADE FOR DENTISTRY and FUGO BLADE FOR PERIPHERAL IRIDOTOMY, MODEL M300.