Orthopaedic Designs, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Orthopaedic Designs, Inc. makes
Orthopaedic Designs, Inc. manufactures orthopedic fixation devices, including self-guiding interlocking nails for long bone stabilization and the ODI compression hip screw system for femoral neck fractures.
These products are classified as Class II devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Ultimate Compression Screw System Ref K972722
Regimes: 510(k) Registry: 510(k)Odi Talon Intramedullary Hip Nail Ref K014189
Regimes: 510(k) Registry: 510(k)Odi 7.0mm Cannulated Screw System Ref K030619
Regimes: 510(k) Registry: 510(k)Self Guiding (Sg) Interlocking Nail Ref K880737
Regimes: 510(k) Registry: 510(k)Odi Ultimate Compression Hip Screw Ref K984331
Regimes: 510(k) Registry: 510(k)Odi Compression Hip Screw System Ref K971993
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthopaedic Designs, Inc. have in the registry?
The registry currently lists 6 devices for Orthopaedic Designs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthopaedic Designs, Inc.'s devices?
Among its 6 most recently registered devices, Orthopaedic Designs, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Orthopaedic Designs, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Orthopaedic Designs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthopaedic Designs, Inc. in the registry?
The most recently registered devices listed for Orthopaedic Designs, Inc. include ULTIMATE COMPRESSION SCREW SYSTEM, ODI TALON INTRAMEDULLARY HIP NAIL, ODI 7.0MM CANNULATED SCREW SYSTEM and SELF GUIDING (SG) INTERLOCKING NAIL.