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Sign in to claim this brandAdvanced Back Technologies
US
Last updated May 23, 2026
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- US
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Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Extentrac Elite | M100 | FDA UDI | Class II | Active |
| Extentrac Elite | K031996 | FDA 510(k) | Class II | Active |
| Extentrac | K980021 | FDA 510(k) | Class II | Active |
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 13, 2015 | Z-1717-2015 | — | terminated | Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs |
| May 13, 2015 | Z-1718-2015 | — | terminated | Item is marketed for use in patients weighing up to 350 lbs, but the device was only approved for use in patients up to 300 lbs |