Ron-Tech Medical, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Ron-Tech Medical, Ltd. makes
Ron-Tech Medical, Ltd. manufactures transvaginal ultrasound probe holder devices and systems, designed to stabilize and position ultrasound probes during pelvic examinations.
These products are classified as Class II medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Transvaginal Ultrasound Probe Holder Device Ref K992071
Regimes: 510(k) Registry: 510(k)Transvaginal Ultrasound Probe Holder System Ref K032585
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ron-Tech Medical, Ltd. have in the registry?
The registry currently lists 2 devices for Ron-Tech Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ron-Tech Medical, Ltd.'s devices?
Among its 2 most recently registered devices, Ron-Tech Medical, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ron-Tech Medical, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ron-Tech Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ron-Tech Medical, Ltd. in the registry?
The most recently registered devices listed for Ron-Tech Medical, Ltd. include TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE and TRANSVAGINAL ULTRASOUND PROBE HOLDER SYSTEM.