Ventrex, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Ventrex, Inc. makes
Ventrex, Inc. manufactures medical devices including allergen discs for diagnostic testing, a tocodynamometer (Featherlite Aqua) for monitoring fetal heart activity, and protective sheaths (Coverox) for obstetric procedures. The portfolio also includes a portable tocodynamometer (Toco Lite, Model TD-01) designed for fetal heart rate monitoring.
The company’s devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. These products are intended for use in the United States.
Catalogue
Ventrex Oxygen Sensor Ref K963415
Regimes: 510(k) Registry: 510(k)Ventrex Allergen Disc Ref K925044
Regimes: 510(k) Registry: 510(k)Featherlite Aqua Tocodynamometer Ref K061044
Regimes: 510(k) Registry: 510(k)Ventrex Allergen Disc Ref K924119
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Toco Lite, Model Td-01 Ref K013477
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ventrex, Inc. have in the registry?
The registry currently lists 6 devices for Ventrex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ventrex, Inc.'s devices?
Among its 6 most recently registered devices, Ventrex, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Ventrex, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Ventrex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ventrex, Inc. in the registry?
The most recently registered devices listed for Ventrex, Inc. include VENTREX OXYGEN SENSOR, VENTREX ALLERGEN DISC, FEATHERLITE AQUA TOCODYNAMOMETER and COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67.