Triopsy Medical, Inc.
Country not established
- Devices
- 1
What Triopsy Medical, Inc. makes
Triopsy Medical, Inc. manufactures biopsy-related devices, including the Triopsy Actuator and two variants of the Triopsy Biopsy Needle (BN-1825-36-01 and BN-1825-55-01), designed for tissue sampling procedures.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01) Ref K242228
510(k) 510(k)
Frequently asked questions
How many devices does Triopsy Medical, Inc. have in the registry?
The registry currently lists 1 device for Triopsy Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Triopsy Medical, Inc.'s devices?
Among its 1 most recently registered device, Triopsy Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Triopsy Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Triopsy Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Triopsy Medical, Inc. in the registry?
The most recently registered devices listed for Triopsy Medical, Inc. include Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01).