510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K970116Substantially Equivalent

Esg-1 Electrosonogram (Esg-1)

Myo-Tronics, Inc., Tukwila WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970116 is the FDA 510(k) clearance record for ESG-1 ELECTROSONOGRAM (ESG-1), a class I device, cleared for Myo-Tronics, Inc. on under FDA product code NFQ (Device, Dental Sonography, For Monitoring Jaw Sounds). FDA records list 6 510(k) clearances for Myo-Tronics, Inc., from to . As of , FDA records show no recalls naming K970116.

Clearance record

Decision date
Received
(79 days to decision)
Product code
NFQ Device, Dental Sonography, For Monitoring Jaw Sounds
Regulation
21 CFR 872.2050
Device class
Class I
Review panel
Dental
Applicant
Myo-Tronics, Inc. 15425 - 33rd Ave. S., Tukwila WA
510(k) summary
Summary
Third party review
No

Clearances, product code NFQ

Trailing 12 months

FDA records hold no clearances under product code NFQ in the trailing twelve months.

FDA records show no clearances under product code NFQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NFQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260