510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K233485Substantially Equivalent

M-Wave

Altivera Medical, Inc., Englewood CO / Abbreviated, Substantially Equivalent
FDA source (opens on fda.gov)

K233485 is the FDA 510(k) clearance record for M-Wave, a class II device, cleared for Zynex Medical, Inc. on under FDA product code IPF (Stimulator, Muscle, Powered). FDA records list 5 510(k) clearances for Altivera Medical, Inc., from to . As of , FDA records show no recalls naming K233485.

Clearance record

Decision date
Received
(91 days to decision)
Product code
IPF Stimulator, Muscle, Powered
Regulation
21 CFR 890.5850
Device class
Class II
Review panel
Physical Medicine
Applicant
Zynex Medical, Inc. 9655 Maroon Cir., Englewood CO
510(k) summary
Statement
Third party review
No

Clearances, product code IPF

Trailing 12 months
3 clearances under product code IPF in the twelve months to October 2026, June 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IPF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20262
July 20260
August 20260
September 20260
October 20260