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 devicesDeviceDevice · Authorizations Verified Status Regime Registry Class
Orthomet Wire For Suture, Cerclage Ref K874919
Regimes: 510(k) Registry: 510(k)Omknee System, Porous Coated Ref K854943
Regimes: 510(k) Registry: 510(k)Perfecta Ii Total Hip System Ref K883618
Regimes: 510(k) Registry: 510(k)Perfecta Total Hip System Ref K903635
Regimes: 510(k) Registry: 510(k)Orthomet Bone Plates Ref K875086
Regimes: 510(k) Registry: 510(k)Perfecta Pda Total Hip System Ref K915795
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Proforma/Ps Total Hip System Ref K880435
Regimes: 510(k) Registry: 510(k)Perfecta Total Hip System, Hemi-Head Component Ref K915868
Regimes: 510(k) Registry: 510(k)Psk Femoral And Tibial Insert Component Ref K920426
Regimes: 510(k) Registry: 510(k)
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