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MES 9000 Muscle Tester

Model Muscle Tester · MYOTRONICS NOROMED, INC · DI D792N9600A0

HCC — Device, Biofeedback · Class II · 21 CFR 882.5050

KZM — Device, Muscle Monitoring · Class II · 21 CFR 890.1375

UDILibrary device dossier · generated 2026-09-12 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

23562019-03: 0 reports for this device; peer average 6/device2024-07: 0 reports for this device; peer average 1/device0307
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0306
2024-0701
This device (reports/month)Average device in HCC, KZM (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — MYOTRONICS NOROMED, INC

  • Warning Letter 2012-04-09 Myotronics-Noromed Inc
  • Warning Letter 2012-04-09 Myotronics-Noromed Inc
  • NAI 2017-03-15 Myotronics-Noromed Inc · 0 citations
  • NAI 2017-03-15 Myotronics-Noromed Inc · 0 citations
  • NAI 2013-11-20 Myotronics-Noromed Inc · 0 citations
  • NAI 2013-11-20 Myotronics-Noromed Inc · 0 citations
  • NAI 2012-07-24 Myotronics-Noromed Inc · 0 citations
  • NAI 2012-07-24 Myotronics-Noromed Inc · 0 citations
  • OAI 2011-05-12 Myotronics-Noromed Inc · 2 citations
  • OAI 2011-05-12 Myotronics-Noromed Inc · 2 citations