Tactile Technologies, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
What Tactile Technologies, Ltd. makes
Tactile Technologies, Ltd. develops implant location software tools designed to assist in identifying and tracking the position of implanted medical devices within the body. These solutions include software variants tailored for specific use cases, such as surgical planning and postoperative verification.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) clearance pathway. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Implant Location Software, Model 0.1.0 Ref K050341
Regimes: 510(k) Registry: 510(k)Implant Location Software-T Ref K070713
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tactile Technologies, Ltd. have in the registry?
The registry currently lists 2 devices for Tactile Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tactile Technologies, Ltd.'s devices?
Among its 2 most recently registered devices, Tactile Technologies, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tactile Technologies, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tactile Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tactile Technologies, Ltd. in the registry?
The most recently registered devices listed for Tactile Technologies, Ltd. include IMPLANT LOCATION SOFTWARE, MODEL 0.1.0 and IMPLANT LOCATION SOFTWARE-T.