510(k) Report

FDA applicant

Mettler Electronics Corp.

Anaheim, CA34 decisions1985–20241 recall

FDA records 34 decisions for Mettler Electronics Corp. (Anaheim, CA) from 1985 to 2024: 34 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IMI (Ultrasonic Diathermy For Use In Applying…). Its devices cite 19 predicates, 7 of them its own earlier devices. 1 recall is linked to its devices.

FDA’s records also spell it “Mettler Electronics Corporation”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Mettler Electronics Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2007: 12009: 12011: 12012: 12023: 12024: 1
2007high 1 (2007) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

1in 2011

2011: 1
2007high 1 (2011) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Mettler Electronics Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Mettler Electronics Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • IPFStimulator, Muscle, Powered13decisions
  • IMIUltrasonic Diathermy For Use In Applying Therapeutic Deep Heat7decisions
  • IMGStimulator, Ultrasound And Muscle, For Use In Applying Therapeutic Deep Heat6decisions
  • IMJDiathermy, Shortwave, For Use In Applying Therapeutic Deep Heat2decisions
  • FRNPump, Infusion1decision
  • LIHInterferential Current Therapy1decision

Also: ITH (1), GZJ (1), ILY (1), IKK (1).

Whose devices does it build on?

Its devices cite 19 predicates; 7 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 34 times; 7 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K071137Sonicator Plus 940, Model ME940Mettler Electronics Corp. · 20074cite it
  • K013192Sonicator Plus 930, Model ME 930Mettler Electronics Corp. · 20014cite it
  • K031017Sys*Stim 208 and 208AMettler Electronics Corp. · 20034cite it
  • K113017Sys*Stim 240Mettler Electronics Corp. · 20123cite it
  • K042554Auto Therm 390, Model ME 390Mettler Electronics Corp. · 20043cite it
  • K984142Sonicator Plus 992, Model Number ME 992 and Sonicator Plus 994, Model Number ME 994Mettler Electronics Corp. · 19993cite it

What has FDA decided for it lately?

  • K233926accufitMettler Electronics Corporation · 2024
  • K223802accufitMettler Electronics Corporation · 2023
  • K113017Sys*Stim 240Mettler Electronics Corp. · 2012
  • K111482Sonicator Plus 920Mettler Electronics Corp. · 2011
  • K091540MTD 4000Mettler Electronics Corp. · 20091 recall
  • K071137Sonicator Plus 940, Model ME940Mettler Electronics Corp. · 2007
  • K053546Sonicator 740, Model ME 740Mettler Electronics Corp. · 2006
  • K043586Laser Sys*Stim 540, Model ME 540Mettler Electronics Corp. · 2005

All 32 as Mettler Electronics Corp. →All 2 as Mettler Electronics Corporation →

What has been recalled?

1 recall linked to its devices; the latest:

  • K091540MTD 4000 - Mettler Traction Decompression System, Model: ME 4000 Product Usage: Provide…Apr 14, 2011