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Device, Iontophoresis, Other Uses
FDA product code EGJ · Class 2 · Physical Medicine
145
Registered devices
146
Adverse events
7
Recalls
73
510(k) clearances
Devices with this code
CHATTANOOGA — DJO, LLCTrivarion Small Sample — ACTIVATEK INC.Iontophoresis Dupel Blue Medium - Standard 2.5 mL — EMPI, INC.Dynatron Ion Butterfly — Dynatronics CorporationTrivarion Medium & Butterfly Sample — ACTIVATEK INC.Drionic TM — GENERAL MEDICAL COMPANYCHATTANOOGA — DJO, LLCDrionic TM — GENERAL MEDICAL COMPANYDrionic TM — GENERAL MEDICAL COMPANYDERMADRY — Dermadry Laboratories IncTrivarion — ACTIVATEK INC.ActivaTek Ionto4 Kit — NORTH COAST MEDICAL, INC.Ionto480 Buffered Iontophoresis Electrode Treatment Kit — AXELGAARD MANUFACTURING CO., LTD.Ionto480 Buffered Iontophoresis Electrode Treatment Kit — AXELGAARD MANUFACTURING CO., LTD.CHATTANOOGA — DJO, LLCCHATTANOOGA — DJO, LLCDynatron iBOX2 — Dynatronics CorporationActivaTek Ionto4 Kit — NORTH COAST MEDICAL, INC.BodyMed Iontophoresis Electrode Kit — COMPASS HEALTH BRANDS CORP.Dynatron® ion™ Medium — Dynatronics CorporationRichmar — South Dakota Partners Inc.Drionic TM — GENERAL MEDICAL COMPANYDrionic TM — GENERAL MEDICAL COMPANYDrionic TM — GENERAL MEDICAL COMPANY
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-05-22 | LTS Therapy Systems, LLC | The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device. |
| 2025-05-22 | LTS Therapy Systems, LLC | The nonwoven pads in the device do not absorb the saline solution or any other liquid intended to be used with the device. |
| 2021-11-10 | Tapemark Company | The dosage information on the pouch is incorrect; the primary carton label is correct. |
| 2017-01-30 | Hidrex GmbH | The device was reclassified from a class III device to a class II device and there are new documentation requirements. |
| 2017-01-30 | Hidrex GmbH | The device was reclassified from a class III device to a class II device and there are new documentation requirements. |
| 2017-01-30 | Hidrex GmbH | The device was reclassified from a class III device to a class II device and there are new documentation requirements. |
| 2005-03-15 | Selectivemed Components Inc | The conductor portion of the electrode is installed backwards, with the plastic and silver portions of the electrode reversed. |
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