GWXClass I

Fork, Tuning

21 CFR 882.1525 / Neurology

GWX is the FDA product code for Fork, Tuning, a class I device type, regulated under 21 CFR 882.1525. As of 2026-09-10, FDA records hold 4 510(k) clearances under this code, the most recent dated 1988-01-04, and no recalls.

Classification record

Product code: GWX
Device name: Fork, Tuning
Regulation: 21 CFR 882.1525
Device class: Class I
Review panel: Neurology
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: Yes
Third party review eligible: No
Ingested clearances: 4
Ingested recalls: 0

Clearances, product code GWX

By decision year

4 clearances under product code GWX with a decision year between 1976 and 1988, 1976 the highest year at 2.

Show the numbers

510(k) clearances under FDA product code GWX by decision year
Year	Clearances
1976	2
1981	1
1988	1

Applicants with the most clearances

Product code GWX

Applicants holding the most 510(k) clearances under product code GWX
Applicant	Clearances
Fred Sammons, Inc.	2
Conphar, Inc.	1
Solway, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 124 companies shown, in name order

Recent clearances

Product code GWX

Recent recalls

Product code GWX

FDA records show no recalls under product code GWX.

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)