Takiron Co., Ltd.
JapanFDA applicant, unverified
- Devices
- 6
What Takiron Co., Ltd. makes
Takiron Co., Ltd. manufactures orthopedic fixation devices, including intramedullary pins, screws, and bioabsorbable bone fixation systems designed for internal stabilization of fractures. Their product line also includes a porous titanium implant, COMPORUS, intended for bone integration and load-bearing applications in orthopedic surgery.
These devices are classified as Class II under US regulations and are listed via the FDA’s 510(k) pathway. The company operates from the United States, adhering to regulatory requirements for medical devices in that jurisdiction.
Catalogue
Osteotrans-Ot Pin Ref K073311
Regimes: 510(k) Registry: 510(k)Osteotrans-Ot Screw Ref K073312
Regimes: 510(k) Registry: 510(k)Bioactif Osteotrans Interfence Screw Ref K081390
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Comporus Ref K062691
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Takiron Co., Ltd. have in the registry?
The registry currently lists 6 devices for Takiron Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Takiron Co., Ltd.'s devices?
Among its 6 most recently registered devices, Takiron Co., Ltd. has devices listed in FDA 510(k) (6 devices).
What risk classes do Takiron Co., Ltd.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Takiron Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Takiron Co., Ltd. in the registry?
The most recently registered devices listed for Takiron Co., Ltd. include OSTEOTRANS-OT PIN, OSTEOTRANS-OT SCREW, BIOACTIF OSTEOTRANS INTERFENCE SCREW and OSTEOTRANS -MX BIOABSORBABLE BONE FIXATION SYSTEM.