Sontra Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Sontra Medical, Inc. makes
Sontra Medical, Inc. manufactures the SONOPREP Impedance Diagnostics (IDX) System, Model D1000, and the SONOPREP Ultrasonic Skin Permeation System and Topical Anesthetic Kit, Model D2000.
These devices are Class II and listed in the FDA 510(k) registry. The company is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sontra Medical, Inc. have in the registry?
The registry currently lists 2 devices for Sontra Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sontra Medical, Inc.'s devices?
Among its 2 most recently registered devices, Sontra Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sontra Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sontra Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sontra Medical, Inc. in the registry?
The most recently registered devices listed for Sontra Medical, Inc. include SONOPREP IMPEDANCE DIAGNOSTICS (IDX) SYSTEM, MODEL D1000 and SONOPREP ULTRASONIC SKIN PERMEATION SYSTEM AND TOPICAL ANESTHETIC KIT, MODEL D2000.