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
IPSClass I

Cane

21 CFR 890.3075 / Physical Medicine
FDA source (opens on fda.gov)

IPS is the FDA product code for Cane, a class I device type, regulated under 21 CFR 890.3075. As of , FDA records hold 9 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
IPS
Device name
Cane
Regulation
21 CFR 890.3075
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
9
Ingested recalls
4

Clearances, product code IPS

By decision year
9 clearances under product code IPS with a decision year between 1977 and 1983, 1979 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code IPS by decision year
YearClearances
19772
19781
19793
19821
19832

Applicants with the most clearances

Product code IPS
Applicants holding the most 510(k) clearances under product code IPS
ApplicantClearances
Maddak, Inc.4
Fred Sammons, Inc.1
Guardian Products Co., Inc.1
Manuco Manufacturing Co., Inc.1
Med Fusion Systems, Inc.1
Union Carbide Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 166 companies shown, in name order