IKXClass I

Aid, Transfer

21 CFR 890.5050 / Physical Medicine

IKX is the FDA product code for Aid, Transfer, a class I device type, regulated under 21 CFR 890.5050. As of 2026-09-10, FDA records hold 18 510(k) clearances under this code, the most recent dated 1986-08-13, and 20 recalls.

Classification record

Product code: IKX
Device name: Aid, Transfer
Regulation: 21 CFR 890.5050
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: 18
Ingested recalls: 20

Clearances, product code IKX

By decision year

18 clearances under product code IKX with a decision year between 1978 and 1986, 1982 the highest year at 6.

Show the numbers

510(k) clearances under FDA product code IKX by decision year
Year	Clearances
1978	3
1979	1
1981	3
1982	6
1983	3
1984	1
1986	1

Applicants with the most clearances

Product code IKX

Applicants holding the most 510(k) clearances under product code IKX
Applicant	Clearances
Fred Sammons, Inc.	8
Guardian Products Co., Inc.	2
Maddak, Inc.	2
Orthion Corp.	2
M. Dahm International ApS	1
Mednet, Inc.	1
Orthopedic Equipment Co., Inc.	1
Taylor Medical Equipment	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 275 companies shown, in name order