Arthrotek/Biomet, Inc.
Country not established
- Devices
- 1
What Arthrotek/Biomet, Inc. makes
Arthrotek/Biomet, Inc. manufactures orthopedic fixation devices, including screw systems for ligament and bone stabilization, such as the WasherLOC, Ligament Screw, and No-Profile Bi-Cortical Screw. The portfolio also includes specialized clamps like the Channel Ligament Clamp and the Heckman Screw, designed for internal joint fixation.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthrotek/Biomet, Inc. have in the registry?
The registry currently lists 1 device for Arthrotek/Biomet, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthrotek/Biomet, Inc.'s devices?
Among its 1 most recently registered device, Arthrotek/Biomet, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Arthrotek/Biomet, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Arthrotek/Biomet, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arthrotek/Biomet, Inc. in the registry?
The most recently registered devices listed for Arthrotek/Biomet, Inc. include WASHERLOC SCREW SYSTEM, LIGAMENT SCREW SYSTEM, NO-PROFILE BI-CORTICAL SCREW SYSTEM, CHANNEL LIGAMENT CLAMP, HECKMAN SCRE.