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Sign in to claim this brandMETTLER ELECTRONICS CORP.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 1333 SOUTH CLAUDINA ST., ANAHEIM, CA, 92805
- Website
- —
- —
- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 2013558
- DUNS Number
- —
Catalogue (91)
Page 1 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Sonigel Lotion with Aloe Vera | 1864 | FDA UDI | Class II | Active |
| EZ Trode, 2.75" round | 2222 | FDA UDI | Class II | Active |
| Sys*Stim 240 | ME 240 | FDA UDI | Class II | Active |
| Sonigel Ultrasound Gel Couplants | 1852 | FDA UDI | Class II | Active |
| Sonigel Ultrasound Gel Couplants | 1853 | FDA UDI | Class II | Active |
| Sonicator Plus 994, 4 channel | ME 994 | FDA UDI | Class II | Active |
| V Trode, 2" square | 2705 | FDA UDI | Class II | Active |
| MTD 4000 Digital Traction | ME 4000 | FDA UDI | Class II | Active |
| Auto*Therm 390 | ME 390 | FDA UDI | Class II | Active |
| Trio*Stim 215 | ME 215 | FDA UDI | Class II | Active |
| Applicator 7335 | 7335 | FDA UDI | Class II | Active |
| Ultrasound Applicator 7413 | 7413 | FDA UDI | Class II | Active |
| Sonicator 740 plus 5 cm2 applicator | ME 740 | FDA UDI | Class II | Active |
| Sonicator Plus 930, 2 channel | ME 930 | FDA UDI | Class II | Active |
| Laser Applicator 5401 | 5401 | FDA UDI | Class II | Active |
| Applicator 9401 | 9401 | FDA UDI | Class II | Active |
| Sonigel Ultrasound Gel Couplants | 1844 | FDA UDI | Class II | Active |
| EZ Trode, 2" round | 2221 | FDA UDI | Class II | Active |
| Tens 210 | ME 210 | FDA UDI | Class II | Active |
| Sonicator 718 | ME 718 | FDA UDI | Class II | Active |
| V Trode, 2.75" round | 2703 | FDA UDI | Class II | Active |
| Sys Stim 294 | ME 294 | FDA UDI | Class II | Active |
| Sonicator Plus 992, 2 channel | ME 992 | FDA UDI | Class II | Active |
| Applicator 7107 | 7107 | FDA UDI | Class II | Active |
| Sys*Stim 228 | ME 228 | FDA UDI | Class II | Active |
| Sonigel Lotion with Aloe Vera | 1863 | FDA UDI | Class II | Active |
| Laser Sys*Stim 540 | ME 540 | FDA UDI | Class II | Active |
| Sys*Stim 206 | ME 206 | FDA UDI | Class II | Active |
| Sonigel Ultrasound Gel Couplants | 1851 | FDA UDI | Class II | Active |
| Tens 210t | ME 210T | FDA UDI | Class II | Active |
| Sonicator 719 | ME 719 | FDA UDI | Class II | Active |
| Applicator 7513 | 7513 | FDA UDI | Class II | Active |
| Ultrasound Applicator 7431 | 7431 | FDA UDI | Class II | Active |
| Cluster Applicator 5402 | 5402 | FDA UDI | Class II | Active |
| Silberg T.P.S. | ME 800 | FDA UDI | Class II | Active |
| EZ Trode, 2" x 5" rectangular | 2223 | FDA UDI | Class II | Active |
| Sys*Stim 208, one channel | ME 208 | FDA UDI | Class II | Active |
| Ultrasound Applicator 7410 | 7410 | FDA UDI | Class II | Active |
| Applicator 7305 | 7305 | FDA UDI | Class II | Active |
| Tens 212 | ME 212 | FDA UDI | Class II | Active |
| Applicator 7005 | 7005 | FDA UDI | Class II | Active |
| Applicator 9402 | 9402 | FDA UDI | Class II | Active |
| Sonicator Plus 920 | ME 920 | FDA UDI | Class II | Active |
| Laser Applicator 2401 | 2401 | FDA UDI | Class II | Active |
| Applicator 7331 | 7331 | FDA UDI | Class II | Active |
| Sonicator Plus 940, 4 channel | ME 940 | FDA UDI | Class II | Active |
| Drum Applicator 3980 | 3980 | FDA UDI | Class II | Active |
| V Trode, 2" x 4" oval | 2704 | FDA UDI | Class II | Active |
| Applicator 7310 | 7310 | FDA UDI | Class II | Active |
| Cluster Applicator 2402 | 2402 | FDA UDI | Class II | Active |
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FDA Recalls (1)
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 |
|---|---|---|---|---|
| Apr 14, 2011 | Z-2580-2011 | — | terminated | The recall was initiated because Mettler has confirmed the possible failure of internal mechanical component and software detection for potential failure regarding Electronics Traction Device - MTD4000. The firm are initiating the recall because component failure might result in patient injury. Use of the device should cease immediately. |