Ecton, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Ecton, Inc. makes
Ecton, Inc. manufactures ultrasound systems, including the ECTON LYNX and LYNX ULTRASOUND SYSTEM, designed for diagnostic imaging in medical settings. These devices are intended for real-time visualization of internal body structures, supporting clinical assessments in various specialties such as obstetrics, cardiology, and general surgery.
The company’s ultrasound systems fall under FDA Class II regulatory classification and are authorised through the 510(k) clearance process. These devices are listed in the FDA’s 510(k) registry, adhering to US medical device regulations. The manufacturer is based in the United States.
Catalogue
Ecton Lynx Ultrasound System Ref K982800
Regimes: 510(k) Registry: 510(k)Lynx Ultrasound System Ref K991872
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ecton, Inc. have in the registry?
The registry currently lists 2 devices for Ecton, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ecton, Inc.'s devices?
Among its 2 most recently registered devices, Ecton, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ecton, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ecton, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ecton, Inc. in the registry?
The most recently registered devices listed for Ecton, Inc. include ECTON LYNX ULTRASOUND SYSTEM and LYNX ULTRASOUND SYSTEM.