Ultraguide, Ltd.
Country not established
- Devices
- 6
What Ultraguide, Ltd. makes
Ultraguide, Ltd. manufactures image-guided surgical navigation systems designed for real-time tracking during computed tomography (CT) and magnetic resonance imaging (MRI) procedures. Their devices include CT-GUIDE 1010 and CTG 2000SA for CT-based interventions, as well as MR-GUIDE 2000 and MR-GUIDE 3000 for MRI-guided applications. The USG 2000SA and ULTRAGUIDE 1000 support ultrasound-assisted procedures. These systems are intended for precise localization and guidance in minimally invasive surgeries.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Ultraguide Ct-Guide 1010 Ref K002258
Regimes: 510(k) Registry: 510(k)Ultraguide Ctg 2000SA Ref K022354
Regimes: 510(k) Registry: 510(k)Mr-Guide 2000 Ref K013150
Regimes: 510(k) Registry: 510(k)Ultraguide Mr-Guide 3000 Ref K011418
Regimes: 510(k) Registry: 510(k)Usg 2000SA Ref K023227
Regimes: 510(k) Registry: 510(k)Ultraguide 1000 Ref K974432
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultraguide, Ltd. have in the registry?
The registry currently lists 6 devices for Ultraguide, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultraguide, Ltd.'s devices?
Among its 6 most recently registered devices, Ultraguide, Ltd. has devices listed in FDA 510(k) (6 devices).
What risk classes do Ultraguide, Ltd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Ultraguide, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultraguide, Ltd. in the registry?
The most recently registered devices listed for Ultraguide, Ltd. include ULTRAGUIDE CT-GUIDE 1010, ULTRAGUIDE CTG 2000SA, MR-GUIDE 2000 and ULTRAGUIDE MR-GUIDE 3000.