Surgivision, Inc.
United StatesFDA applicant, unverified
- Devices
- 13
What Surgivision, Inc. makes
Surgivision, Inc. manufactures surgical accessories and equipment designed for neurosurgical and MRI-compatible procedures, including the Clearpoint System for intraoperative imaging guidance, MRI-compatible neuro drapes, head fixation arcs and table bases for precise patient positioning, and ventricular cannulas compatible with MRI environments.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the 510(k) clearance pathway. These products are intended for use in the United States, where the manufacturer is based.
Catalogue
Search and filter all 13 devicesFrequently asked questions
How many devices does Surgivision, Inc. have in the registry?
The registry currently lists 13 devices for Surgivision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Surgivision, Inc.'s devices?
Among its 13 most recently registered devices, Surgivision, Inc. has devices listed in FDA 510(k) (13 devices).
What risk classes do Surgivision, Inc.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Surgivision, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Surgivision, Inc. in the registry?
The most recently registered devices listed for Surgivision, Inc. include CLEARPOINT SYSTEM, INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR INTERNAL MR COIL, ENDO-ESOPHAGEAL MR COIL and MRI NEURO DRAPE.