ILIClass I

Sling, Arm

21 CFR 890.3640 / Physical Medicine

ILI is the FDA product code for Sling, Arm, a class I device type, regulated under 21 CFR 890.3640. As of 2026-09-10, FDA records hold 21 510(k) clearances under this code, the most recent dated 1991-08-21, and 5 recalls.

Classification record

Product code: ILI
Device name: Sling, Arm
Regulation: 21 CFR 890.3640
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: 21
Ingested recalls: 5

Clearances, product code ILI

By decision year

21 clearances under product code ILI with a decision year between 1976 and 1991, 1981 the highest year at 6.

Show the numbers

510(k) clearances under FDA product code ILI by decision year
Year	Clearances
1976	2
1977	1
1980	4
1981	6
1982	3
1983	4
1991	1

Applicants with the most clearances

Product code ILI

Applicants holding the most 510(k) clearances under product code ILI
Applicant	Clearances
Fred Sammons, Inc.	3
Maddak, Inc.	3
Danek Medical, Inc.	2
The Owenby Co.	2
Warm & Form, Orthopedic Materials	2
Abco Dealers, Inc.	1
BD Becton Dickinson Vacutainer Systems Preanalytic	1
Conphar, Inc.	1
Food and Drug Service, Inc.	1
Johnson & Johnson Professionals, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 327 companies shown, in name order