Stebar Instrument Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Stebar Instrument Corp. makes
Stebar Instrument Corp. manufactures the Schroeder oral/nasal directional stylette, a medical device designed for guiding endotracheal tubes or other tubular instruments through the oral or nasal passages during intubation procedures.
The company’s products fall under FDA Class I regulation and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Schroeder Oral/Nasal Directional Stylette Ref K952266
Regimes: 510(k) Registry: 510(k)Schroeder Oral/Nasal Directional Stylette Ref K935797
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stebar Instrument Corp. have in the registry?
The registry currently lists 2 devices for Stebar Instrument Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stebar Instrument Corp.'s devices?
Among its 2 most recently registered devices, Stebar Instrument Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Stebar Instrument Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stebar Instrument Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Stebar Instrument Corp. in the registry?
The most recently registered devices listed for Stebar Instrument Corp. include SCHROEDER ORAL/NASAL DIRECTIONAL STYLETTE.