IQMClass I

Splint, Temporary Training

21 CFR 890.3025 / Physical Medicine

IQM is the FDA product code for Splint, Temporary Training, a class I device type, regulated under 21 CFR 890.3025. As of 2026-09-10, FDA records hold 3 510(k) clearances under this code, the most recent dated 1977-07-21, and no recalls.

Classification record

Product code: IQM
Device name: Splint, Temporary Training
Regulation: 21 CFR 890.3025
Device class: Class I
Review panel: Physical Medicine
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: Yes
Third party review eligible: No
Ingested clearances: 3
Ingested recalls: 0

Clearances, product code IQM

By decision year

3 clearances under product code IQM with a decision year between 1977 and 1977, 1977 the highest year at 3.

Show the numbers

510(k) clearances under FDA product code IQM by decision year
Year	Clearances
1977	3

Applicants with the most clearances

Product code IQM

Applicants holding the most 510(k) clearances under product code IQM
Applicant	Clearances
Mizuho Orthopedic Systems Inc	2
Fred Sammons, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 45 companies shown, in name order

Recent clearances

Product code IQM

Recent recalls

Product code IQM

FDA records show no recalls under product code IQM.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)