510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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IPGClass I

Shoe, Cast

21 CFR 890.3025 / Physical Medicine
FDA source (opens on fda.gov)

IPG is the FDA product code for Shoe, Cast, a class I device type, regulated under 21 CFR 890.3025. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
IPG
Device name
Shoe, Cast
Regulation
21 CFR 890.3025
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
6
Ingested recalls
0

Clearances, product code IPG

By decision year
6 clearances under product code IPG with a decision year between 1976 and 2003, 1976 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code IPG by decision year
YearClearances
19762
19782
19791
20031

Applicants with the most clearances

Product code IPG
Applicants holding the most 510(k) clearances under product code IPG
ApplicantClearances
Ballert Orthopedic Corp.1
Cutler Biomedical1
Ness-Neuromuscular Electrical Stimulation Systems1
Parke-Davis Co.1
Richard'S Medical Equip., Inc.1
Togard, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 91 companies shown, in name order