Truphatek, Ltd.
IsraelFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
Laryngoscope Blades Ref K883414
510(k) 510(k)Oriel Ref K920272
510(k) 510(k)Otoscope Ref K902205
510(k) 510(k)Throat-A-Scope Ref K923227
510(k) 510(k)
Frequently asked questions
How many devices does Truphatek, Ltd. have in the registry?
The registry currently lists 4 devices for Truphatek, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Truphatek, Ltd.'s devices?
Among its 4 most recently registered devices, Truphatek, Ltd. has devices listed in FDA 510(k) (4 devices).
What risk classes do Truphatek, Ltd.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Truphatek, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Truphatek, Ltd. in the registry?
The most recently registered devices listed for Truphatek, Ltd. include LARYNGOSCOPE BLADES, ORIEL, OTOSCOPE and THROAT-A-SCOPE.