Ntero Surgical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Ntero Surgical, Inc. makes
Ntero Surgical, Inc. manufactures radiofrequency ablation devices, including the NTERO RF Sleeve for tissue treatment, as well as the NTERO Nomad and HotRod systems designed for minimally invasive surgical procedures.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The company is based in the United States.
Catalogue
Ntero Rf Sleeve Ref K992572
Regimes: 510(k) Registry: 510(k)Ntero Nomad System Ref K010815
Regimes: 510(k) Registry: 510(k)Ntero Hotrod System Ref K014251
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ntero Surgical, Inc. have in the registry?
The registry currently lists 3 devices for Ntero Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ntero Surgical, Inc.'s devices?
Among its 3 most recently registered devices, Ntero Surgical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ntero Surgical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ntero Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ntero Surgical, Inc. in the registry?
The most recently registered devices listed for Ntero Surgical, Inc. include NTERO RF SLEEVE, NTERO NOMAD SYSTEM and NTERO HOTROD SYSTEM.