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Equipment, Traction, Powered
FDA product code ITH · Class 2 · Physical Medicine
87
Registered devices
53
Adverse events
5
Recalls
71
510(k) clearances
Devices with this code
CHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCDecompression of Choice — PIVOTAL HEALTH SOLUTIONS, INC.SpineMED Decompression System — Universal Pain Technology Canada IncCHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCModpod — HOLLYWOG, LLCCHATTANOOGA — DJO, LLCDecompression of Choice — PIVOTAL HEALTH SOLUTIONS, INC.CHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCclTrac — Zimmer MedizinSysteme GmbHCHATTANOOGA — DJO, LLCAntalgic Trak — ANTALGIC-TRAKExtentrac Elite — Advanced Back Technologies IncTM-400 — ITO CO., LTD.Decompression of Choice — PIVOTAL HEALTH SOLUTIONS, INC.CHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-04-29 | Pivotal Health Solutions, Inc. | This product is being recalled due to potentially insufficient rework on a part (E7130-B) on the lumbar section of the frame on 6 distributed tables. There were |
| 2015-05-13 | Advanced Back Technologies, Inc. | 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 |
| 2015-05-13 | Advanced Back Technologies, Inc. | 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 |
| 2011-08-11 | Spinetronics, LLC | On 08/11/2011 Spinetronics, LLC initiated a recall of Antalgic-Trak Product Brochures which contained language and/or claims that were not cleared under the ori |
| 2011-04-14 | Mettler Electronics Corp | The recall was initiated because Mettler has confirmed the possible failure of internal mechanical component and software detection for potential failure regard |
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