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
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K242525Substantially Equivalent

iTOF®

Nerbio Medical Software Platforms, Inc., San Jose CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K242525 is the FDA 510(k) clearance record for iTOF®, a class II device, cleared for Nerbio Medical Software Platforms, Inc. on under FDA product code KOI (Stimulator, Nerve, Peripheral, Electric). FDA records list one 510(k) clearance for Nerbio Medical Software Platforms, Inc. As of , FDA records show no recalls naming K242525.

Clearance record

Decision date
Received
(101 days to decision)
Product code
KOI Stimulator, Nerve, Peripheral, Electric
Regulation
21 CFR 868.2775
Device class
Class II
Review panel
Anesthesiology
Applicant
Nerbio Medical Software Platforms, Inc. 1900 Camden Ave., San Jose CA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code KOI

Trailing 12 months
1 clearance under product code KOI in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KOI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260