ELEOSRecalls & reported problems across all models
Onkos Surgical, Inc. · 127 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
ELEOS models — page 2
127 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- ELEOS™ 2500CC15EPROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER1 death1 report
- ELEOS™ 2500CP12EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ 2500CP14EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ 2500CP16EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ 25102211EEXTRACTOR1 report
- ELEOS™ 25107000EORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ELEOS™ 25107001EORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ELEOS™ 25107600ETEMPLATE1 report
- ELEOS™ 26000027EProsthesis, hip, semi-constrained (metal cemented acetabular component)1 report
- ELEOS™ 26010002EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ 26010007EPROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- ELEOS™ 26010010EPROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED1 report
- ELEOS™ 26012805EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ BP-1417M-03NTEMPLATE1 report
- ELEOS™ K0001016EORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- ELEOS™ K0002008EEXTRACTOR1 report
- ELEOS™ KPONTP29EPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- ELEOS™ KPONTP38EPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- ELEOS™ KSC10100EPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- ELEOS™ KSP10140EPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- ELEOS™ KSP22100EPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- ELEOS™ KTAGB115EPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- ELEOS™ KTAGB405EPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER1 report
- ELEOS™ MS-050MM-02MProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ SPSE0002EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ SPSE0005EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
- ELEOS™ SPSEB011EProsthesis, hip, semi-constrained, metal/polymer, cemented1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page