THE TMJ APPLIANCE— 510(k) K924974

Name: FDA 510(k) clearance K924974
Creator: U.S. Food and Drug Administration
Published: 1993-06-23

Substantially Equivalent for Some Indications

Myofunctional Research Corp. Pty. , Ltd.

FDA 510(k) clearance K924974 for THE TMJ APPLIANCE, Substantially Equivalent for Some Indications on 1993-06-23. Applicant: Myofunctional Research Corp. Pty. , Ltd.. Device class: 1.

Clearance details

Applicant: Myofunctional Research Corp. Pty. , Ltd.
Product code: Code KMY
Device class: Class 1
Regulation: 21 CFR 872.5525
Advisory panel: Dental
Date received: 1992-09-30
Decision date: 1993-06-23
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Helensvale, Queensland, AU

Download summary PDF View on FDA.gov ↗

Recent devices under product code KMY

view all

K931615 — NITE-GUIDE1995-04-14
K942667 — DENT-O-CRYL ORTHODONTIC ACRYLIC1995-02-13
K924351 — GLENROE ELASTIBITE STIMULATOR1994-01-06
K925064 — RELAX-O-GUARD1993-09-13
K924975 — THE ORTHOTRAINER1993-07-08

Adverse events under product code KMY

product code KMY

Injury: 1,457
Total: 1,457

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.