Bionic Instrument Corp.
Country not established
- Devices
- 1
What Bionic Instrument Corp. makes
Bionic Instrument Corp. manufactures the Klein Wire Tightener, a surgical device used for securing orthopedic wires during procedures such as fracture fixation or bone stabilization.
The company’s portfolio is regulated under FDA’s Class I device classification, with the Klein Wire Tightener listed via a 510(k) submission. The manufacturer is based in the United States.
Catalogue
Klein Wire Tightener/Bionic Wire Ref K833726
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bionic Instrument Corp. have in the registry?
The registry currently lists 1 device for Bionic Instrument Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bionic Instrument Corp.'s devices?
Among its 1 most recently registered device, Bionic Instrument Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Bionic Instrument Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bionic Instrument Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bionic Instrument Corp. in the registry?
The most recently registered devices listed for Bionic Instrument Corp. include KLEIN WIRE TIGHTENER/BIONIC WIRE.