Orthomet, Inc.
United StatesFDA applicant, unverified
- Devices
- 60
What Orthomet, Inc. makes
Orthomet, Inc. manufactures orthopedic implants and instruments including tibial tray PMMA plugs for total knee systems, titanium nitride coated hemi-head components, hybrid femoral stems for total hip systems, spinal frame systems, cannulated screws, femoral stems, bone screws, and anatomically guided carpal tunnel release systems.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Orthomet, Inc. is based in the United States.
Catalogue
Search and filter all 60 devicesShowing 1-50 of 60
Frequently asked questions
How many devices does Orthomet, Inc. have in the registry?
The registry currently lists 60 devices for Orthomet, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orthomet, Inc.'s devices?
Among its 50 most recently registered devices, Orthomet, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Orthomet, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Orthomet, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orthomet, Inc. in the registry?
The most recently registered devices listed for Orthomet, Inc. include TIBIAL TRAY PMMA PLUG FOR PLUS/AXIOM TOTAL KNEE SY, TITANIUM NITRIDE COATED HEMI-HEAD COMPONENT, HYBRID FEMORAL STEM, PERFECTA TOTAL HIP SYSTEM and LEA PLAZA SPINAL FRAME SYSTEM.