Myo-Tronics Research, Inc.

FDA Regulatory Profile

Myo-Tronics Research, Inc. has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Nov 19, 1984

Reviewing Myo-Tronics Research, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Myo-Tronics Research, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances8Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K842223J4 MYO-MONITORNov 19, 1984
K842224BNS 40Nov 19, 1984
K833132MUCOSAL ADJUSTMENT PASTE LIQUID SPRAYFeb 10, 1984
K831364TESTCORP RAMay 27, 1983
K830034MODEL EM-2 BIOELECTRIC PROCESSORFeb 9, 1983
K813533ELECTRIC MUSCLE STIMULATORMar 5, 1982
K810528MODEL EM-IRMar 31, 1981
K770252MONITOR, MYO, MODEL J3Feb 18, 1977

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.