510(k) Report

FDA applicant

Rich-Mar Corp.

Inola, OK43 decisions1976–20040 recalls

FDA records 43 decisions for Rich-Mar Corp. (Inola, OK) from 1976 to 2004: 43 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IMI (Ultrasonic Diathermy For Use In Applying…). No recall is linked to its devices.

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 Rich-Mar Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Rich-Mar Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Rich-Mar”

FDA records each applicant name separately; these may or may not be the same firm.