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METTLER ELECTRONICS CORP.

Last updated September 17, 2026

Information

Country: US
Address: 1333 SOUTH CLAUDINA ST., ANAHEIM, CA, 92805
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 2013558
DUNS Number: —

Catalogue (91)

Page 2 of 2

Device	Model / Reference	Registries	Class	Status
EZ Trode, 2" square	2224	FDA UDI	Class II	Active
Tens*stim 211	ME 211	FDA UDI	Class II	Active
V Trode, 2" round	2702	FDA UDI	Class II	Active
Applicator 7001	7001	FDA UDI	Class II	Active
Sys*Stim 208A, two channel	ME 208A	FDA UDI	Class II	Active
Applicator 9201	9201	FDA UDI	Class II	Active
Applicator 9202	9202	FDA UDI	Class II	Active
Sonicator 730	K943469	FDA 510(k)	Class II	Active
Sys*stim 208 And 208a	K031017	FDA 510(k)	Class II	Active
Sys Stim 226	K964028	FDA 510(k)	Class II	Active
Modified Sonicator 720, Model Me720	K880602	FDA 510(k)	Class II	Active
Silberg T.p.s., Tissue Preparation System, Model Me 800	K023083	FDA 510(k)	Class II	Active
Sonicator 720 (model Me720)	K873812	FDA 510(k)	Class II	Active
accufit	K233926	FDA 510(k)	Class II	Active
Sonicator Plus 930, Model Me 930	K013192	FDA 510(k)	Class II	Active
Laser Sys*stim 540, Model Me 540	K043586	FDA 510(k)	Class II	Active
Sonicator 710 (model Me710)	K880901	FDA 510(k)	Class II	Active
Sys*stim 240	K113017	FDA 510(k)	Class II	Active
Sonicator 740, Model Me 740	K053546	FDA 510(k)	Class II	Active
Sonicator 705 Model Me 705	K851397	FDA 510(k)	Class II	Active
Sonicator 716	K934846	FDA 510(k)	Class II	Active
Cc Rider, Model Me180	K951916	FDA 510(k)	Class II	Active
Sys*stim 220	K883080	FDA 510(k)	Class II	Active
Sonicator Plus 940, Model Me940	K071137	FDA 510(k)	Class II	Active
Sonicator Plus 920	K111482	FDA 510(k)	Class II	Active
Mtd 4000	K091540	FDA 510(k)	Class II	Active
Sonicator Plus 992, Model Number Me 992 And Sonicator Plus 994, Model Number Me 994	K984142	FDA 510(k)	Class II	Active
Auto*therm 395, Model Me 395	K022458	FDA 510(k)	Class II	Active
Sonicator Plus	K921436	FDA 510(k)	Class II	Active
accufit	K223802	FDA 510(k)	Class II	Active
Sys Stim 206 Model Me206	K851735	FDA 510(k)	Class II	Active
Sys*stim 207a	K893879	FDA 510(k)	Class II	Active
Sys*stim 206 (model-Me 206)	K860107	FDA 510(k)	Class II	Active
Sonicator 720 (model Me720)	K883228	FDA 510(k)	Class II	Active
Sonicator 715	K934845	FDA 510(k)	Class II	Active
Auto Therm 390, Model Me 390	K042554	FDA 510(k)	Class II	Active
Sys*stim 206a	K893878	FDA 510(k)	Class II	Active
Midification Sys*stim 207 (model-Me207)	K855249	FDA 510(k)	Class II	Active
Sys Stim 206(model-Me 206) Muscle Stimulator	K850013	FDA 510(k)	Class II	Active
Sys Stim 294, Model Me 294	K984114	FDA 510(k)	Class II	Active
Sys*stim 207 Model Me 207	K853750	FDA 510(k)	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.