Paradigm Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Paradigm Medical, Inc. makes
Paradigm Medical, Inc. manufactures THE PRECISIONIST, a surgical instrument designed for precision-guided procedures, and the MARPP Pressure Monitoring System, a device for real-time intra-operative pressure measurement in medical settings.
The company’s portfolio includes Class I and Class II devices, all of which are subject to FDA 510(k) clearance in the United States. The company is headquartered in the US.
Catalogue
Multifrax Laser System Ref K213332
Regimes: 510(k) Registry: 510(k)The Precisionist Ref K900493
Regimes: 510(k) Registry: 510(k)Marpp Pressure Monitoring System Ref K960725
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paradigm Medical, Inc. have in the registry?
The registry currently lists 3 devices for Paradigm Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paradigm Medical, Inc.'s devices?
Among its 3 most recently registered devices, Paradigm Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Paradigm Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Paradigm Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Paradigm Medical, Inc. in the registry?
The most recently registered devices listed for Paradigm Medical, Inc. include Multifrax Laser System, THE PRECISIONIST and MARPP PRESSURE MONITORING SYSTEM.