SYMPHONYRecalls & reported problems across all models
Medos International Sàrl · 113 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
SYMPHONY models — page 2
113 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- SYMPHONY 1020-40-114SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 1020-40-122SPosterior cervical screw system1 report
- SYMPHONY 1020-40-132SPosterior cervical screw system1 report
- SYMPHONY 1020-40-134SAPPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- SYMPHONY 2020-00-116CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- SYMPHONY 2020-00-134ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- SYMPHONY 2020-00-156SCREWDRIVER1 report
- SYMPHONY 2020-00-157DRIVER, PROSTHESIS1 report
- SYMPHONY 2020-00-158Orthopedic stereotaxic instrument1 report
- SYMPHONY 2020-00-222Orthopedic stereotaxic instrument1 report
- SYMPHONY 2020-22-100ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- SYMPHONY 2020-00-503ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- SYMPHONY 2020-44-101Guide, surgical, instrument1 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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