510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K954136Substantially Equivalent

Matrix Microson 410

Matrix Biokinetics, Inc., North Las Vegas NV / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K954136 is the FDA 510(k) clearance record for MATRIX MICROSON 410, a class II device, cleared for Matrix Biokinetics, Inc. on under FDA product code IMI (Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat). FDA records list one 510(k) clearance for Matrix Biokinetics, Inc. As of , FDA records show no recalls naming K954136.

Clearance record

Decision date
Received
(213 days to decision)
Product code
IMI Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat
Regulation
21 CFR 890.5300
Device class
Class II
Review panel
Physical Medicine
Applicant
Matrix Biokinetics, Inc. 4208 Arcata Way, Unit C, North Las Vegas NV
510(k) summary
Statement
Third party review
No

Clearances, product code IMI

Trailing 12 months

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

FDA records show no clearances under product code IMI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code IMI, 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