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

Orthosis, Sacroiliac, Soft

21 CFR 890.3490 / Physical Medicine
FDA source (opens on fda.gov)

IPW is the FDA product code for Orthosis, Sacroiliac, Soft, a class I device type, regulated under 21 CFR 890.3490. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
IPW
Device name
Orthosis, Sacroiliac, Soft
Regulation
21 CFR 890.3490
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
1
Ingested recalls
0

Clearances, product code IPW

By decision year
1 clearance under product code IPW with a decision year between 1981 and 1981, 1981 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code IPW by decision year
YearClearances
19811

Applicants with the most clearances

Product code IPW
Applicants holding the most 510(k) clearances under product code IPW
ApplicantClearances
The Tiggs Co.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 52 companies shown, in name order