Orthopeasia Co., Ltd.
ThailandFDA applicant, unverified
- Devices
- 1
What Orthopeasia Co., Ltd. makes
Orthopeasia Co., Ltd. manufactures the Orthopeasia Spinal Fixation System, a device designed for internal spinal stabilization and fusion procedures.
The company’s spinal fixation system is classified as Class II under FDA regulations and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Orthopeasia Spinal Fixation System Ref K240180
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orthopeasia Co., Ltd. have in the registry?
The registry currently lists 1 device for Orthopeasia Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthopeasia Co., Ltd.'s devices?
Among its 1 most recently registered device, Orthopeasia Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Orthopeasia Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orthopeasia Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthopeasia Co., Ltd. in the registry?
The most recently registered devices listed for Orthopeasia Co., Ltd. include Orthopeasia Spinal Fixation System.