Teknor Medical Products, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Teknor Medical Products, Inc. makes
Teknor Medical Products, Inc. manufactures medical connectors and airway extensions for respiratory applications, as well as breathing filters designed to improve airway management and ventilation safety.
Their products are regulated under FDA 510(k) clearance as Class I and Class II devices, with listings in the U.S. regulatory database. The company is based in the United States.
Catalogue
Connectors And Airway Extensions Ref K931216
Regimes: 510(k) Registry: 510(k)Breathing Filter Ref K931217
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Teknor Medical Products, Inc. have in the registry?
The registry currently lists 2 devices for Teknor Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teknor Medical Products, Inc.'s devices?
Among its 2 most recently registered devices, Teknor Medical Products, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Teknor Medical Products, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Teknor Medical Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teknor Medical Products, Inc. in the registry?
The most recently registered devices listed for Teknor Medical Products, Inc. include CONNECTORS AND AIRWAY EXTENSIONS and BREATHING FILTER.