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
SUBSCRIBE / SIGN IN
ILZClass I

Accessories, Traction

21 CFR 890.5925 / Physical Medicine
FDA source (opens on fda.gov)

ILZ is the FDA product code for Accessories, Traction, a class I device type, regulated under 21 CFR 890.5925. As of , FDA records hold 15 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
ILZ
Device name
Accessories, Traction
Regulation
21 CFR 890.5925
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
15
Ingested recalls
0

Clearances, product code ILZ

By decision year
15 clearances under product code ILZ with a decision year between 1977 and 1992, 1978 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code ILZ by decision year
YearClearances
19771
19783
19791
19823
19832
19852
19892
19921

Applicants with the most clearances

Product code ILZ
Applicants holding the most 510(k) clearances under product code ILZ
ApplicantClearances
Zimmer GmbH3
Warm & Form, Orthopedic Materials3
Altoona Medical Supply1
Chattanooga Group, Inc.1
D.C. Medical Device, Inc.1
Dr. K.G. Rude1
Dyna-Med1
Jerome Medical1
Powlan Manufacturing Co.1
Vibra-Trac Industries1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 41 companies shown, in name order