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Sign in to claim this brandEmsi
US
Last updated May 23, 2026
What Emsi makes
Emsi manufactures transcutaneous electrical stimulation electrodes, physical therapy transcutaneous neuromuscular electrical stimulation systems, knee support orthoses, and lumbar spine orthoses. Their specific products include the EMSI 40 x 40 Electrode, Hypoallergenic Electrode 2x2 4pk, Flex-TENS, Pro-Fit Knee Brace-Large Size, and various other electrode and brace models.
Emsi's devices are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What medical devices does Emsi manufacture?
Emsi manufactures transcutaneous electrical stimulation electrodes, physical therapy transcutaneous neuromuscular electrical stimulation systems, knee support orthoses, and lumbar spine orthoses. Their specific products include electrodes like the EMSI 40 x 40 Electrode and Hypoallergenic Electrode 2x2 4pk, as well as braces like the Pro-Fit Knee Brace-Large Size.
Where is Emsi based?
Emsi is based in the United States. The company operates within the US, manufacturing and distributing its medical devices to healthcare providers and patients across the country.
Which regulatory registries list Emsi's devices?
Emsi's devices are listed in the FDA 510(k) and FDA UDI registries. These registries track medical devices that have been notified to the FDA, ensuring they meet regulatory requirements before being marketed in the United States.
How are Emsi's devices classified?
Emsi's devices are regulated as Class I and Class II medical devices. Class I devices pose the lowest risk and are subject to general controls, while Class II devices require special controls in addition to general controls to ensure their safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 932471881
Catalogue (120)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| EMSI 40 x 40 Electrode | ELEC0012 | FDA UDI | Class II | Active |
| Hypoallergenic Electrode 2x2 4pk | BF5050 | FDA UDI | Class II | Active |
| Flex-TENS Retail 022017 | FLET0001R02 | FDA UDI | Class II | Unknown |
| 25R(4)H-Samples | SRELEC0001 | FDA UDI | Class II | Active |
| Flex-TENS | FLET0001 | FDA UDI | Class II | Active |
| Flex Gar Sock | SOCK0001 | FDA UDI | Class II | Active |
| Electrode 1 Inch Round 4 PK | SRELEC0001B | FDA UDI | Class II | Active |
| Tmr-Garm-Sock9900000 | S9000 | FDA UDI | Class II | Active |
| TMR-ELEC-20402211 2 x 3.9 Foam Electrode | C2211 | FDA UDI | Class II | Active |
| EMSI 1 4 x 7 electrode, 2 2x4 oval | ELEC0014 | FDA UDI | Class II | Unknown |
| Tmr-Elec-20201311 | A1311 | FDA UDI | Class II | Active |
| Ems-5000d | E5000 | FDA UDI | Class II | Active |
| Tens 2500 | TENS-2500D | FDA UDI | Class II | Active |
| Pro-Fit Knee Brace-Large Size | FLEBKX0001 – Large Pro- Fit | FDA UDI | Class I | Active |
| Flex-IT | FLEI0001 | FDA UDI | Class II | Active |
| Tmr-Garm-Knee9900000 | K9000 | FDA UDI | Class II | Active |
| TMR-ELEC-20404211 2 x 4 Oval Electrode | B4211 | FDA UDI | Class II | Active |
| EMSI 4 x 7 Dispersive Pad | ELEC407001 | FDA UDI | Class II | Active |
| TMR-ELEC-20201221 2 x 2 WH Electrode | A1221 | FDA UDI | Class II | Active |
| EMSI 2 x 2 Electrical Stimulation Electrode | ELEC0002 | FDA UDI | Class II | Active |
| Tens 8000 | EMS-DT7202B | FDA UDI | Class II | Active |
| Tmr-Garm-Back9900000 | B9000 | FDA UDI | Class II | Active |
| Electrode 4.0 x 7.0- Dispersive | ELEC407001B | FDA UDI | Class II | Active |
| TMR-ELEC-20352211 2 x 3.5 Foam Electrode | E2211 | FDA UDI | Class II | Active |
| Velect0001b | A001B | FDA UDI | Class II | Active |
| 50R(4)H-Sample | SRELEC0002 | FDA UDI | Class II | Active |
| EMSI Large Velcro Electrical Stimulation Electrode | VELECT0001 | FDA UDI | Class II | Active |
| EMSI 1.75 x 1.75 4 pack Samples | SRELEC0016 | FDA UDI | Class II | Unknown |
| Electrode 1.75 x 1.75 4 pack | ELEC0008B | FDA UDI | Class II | Active |
| Tmr-Garm-Glov9901000 | G0100 | FDA UDI | Class II | Active |
| Velect0002b | A002B | FDA UDI | Class II | Active |
| EMSI 45 x 45 Electrode 4 pack | ELEC0008 | FDA UDI | Class II | Active |
| TMR-ELEC-40605321 4 x 6 WH, DLX Electrode | A5321 | FDA UDI | Class II | Active |
| TMR-ELEC-20402431 2 x 4 Tricot Electrode | A2431 | FDA UDI | Class II | Active |
| PMX2x2 | A0PMX | FDA UDI | Class II | Active |
| TMR-ELEC-20201431 TRICOT HYPO Electrode | A1431 | FDA UDI | Class II | Active |
| Tmr-Garm-Slee9900000 | SL900 | FDA UDI | Class II | Active |
| Flex Gar Glove | GLOV0001 | FDA UDI | Class II | Active |
| TMR-ELEC-15352221 1.5 x 3.5 WH Electrode | A2221 | FDA UDI | Class II | Active |
| Tmr-Elec-20201121 | B1121 | FDA UDI | Class II | Active |
| Flex-MI with Electrodes | FLEMC0001 | FDA UDI | Class II | Active |
| EMSI 40 x 40 Electrical Stimulation Electrode 4 pack | ELEC0001 | FDA UDI | Class II | Active |
| TMR-ELEC-30003421 3 IN RND Hypo Electrode | A3421 | FDA UDI | Class II | Active |
| PM2x2s | A0PMS | FDA UDI | Class II | Active |
| TMR-ELEC-22252122 2.2 x 2.5 Disposable Electrode | A2122 | FDA UDI | Class II | Active |
| Tmr-Elec-30003321 | B3321 | FDA UDI | Class II | Active |
| TMR-ELEC-20003421 2 IN RND, HYPO Electrode | B3421 | FDA UDI | Class II | Active |
| Electrode 1.75 Inch Square | SRELEC0016B | FDA UDI | Class II | Active |
| Flex-IT Retail | FLEI0001R | FDA UDI | Class II | Active |
| Flex-MI | FLEMC0001 | FDA UDI | Class II | Active |
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