Nuortho Surgical, Inc.
Country not established
- Devices
- 1
What Nuortho Surgical, Inc. makes
Nuortho Surgical, Inc. manufactures the Ceruleau Electrosurgical Probe, a device designed for precise tissue cutting and coagulation in surgical procedures.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. Nuortho Surgical, Inc. is based in the United States.
Catalogue
Ceruleau Electrosurgical Probe Ref K101711
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nuortho Surgical, Inc. have in the registry?
The registry currently lists 1 device for Nuortho Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nuortho Surgical, Inc.'s devices?
Among its 1 most recently registered device, Nuortho Surgical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nuortho Surgical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nuortho Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nuortho Surgical, Inc. in the registry?
The most recently registered devices listed for Nuortho Surgical, Inc. include CERULEAU ELECTROSURGICAL PROBE.