Techbopulm, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
What Techbopulm, Ltd. makes
Techbopulm, Ltd. manufactures the STS, a device designed for bronchoscopic procedures to assist in airway management and diagnostic sampling within the respiratory tract.
The company’s portfolio is regulated under Class II medical devices in the United States, with the STS authorised via the FDA’s 510(k) pathway. The manufacturer is based in the US.
Catalogue
Sts Ref K240293
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Techbopulm, Ltd. have in the registry?
The registry currently lists 1 device for Techbopulm, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Techbopulm, Ltd.'s devices?
Among its 1 most recently registered device, Techbopulm, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Techbopulm, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Techbopulm, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Techbopulm, Ltd. in the registry?
The most recently registered devices listed for Techbopulm, Ltd. include STS.