Field Orthopaedics
AustraliaFDA applicant, unverified FDA FEI 3015131017
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Field Orthopaedics makes
Field Orthopaedics manufactures the Extremity All Suture System, a device designed for orthopaedic applications in extremity surgery, utilizing suture-based fixation techniques.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Extremity All Suture System Ref K241695
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3015131017
- Address
- 30 Florence Street, Teneriffe Queensland
Frequently asked questions
How many devices does Field Orthopaedics have in the registry?
The registry currently lists 1 device for Field Orthopaedics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Field Orthopaedics's devices?
Among its 1 most recently registered device, Field Orthopaedics has devices listed in FDA 510(k) (1 device).
What risk classes do Field Orthopaedics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Field Orthopaedics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Field Orthopaedics in the registry?
The most recently registered devices listed for Field Orthopaedics include Extremity All Suture System.