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

Support, Hernia

21 CFR 876.5970 / Gastroenterology, Urology
FDA source (opens on fda.gov)

EXN is the FDA product code for Support, Hernia, a class I device type, regulated under 21 CFR 876.5970. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
EXN
Device name
Support, Hernia
Regulation
21 CFR 876.5970
Device class
Class I
Review panel
Gastroenterology, Urology
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 EXN

By decision year
1 clearance under product code EXN with a decision year between 1990 and 1990, 1990 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code EXN by decision year
YearClearances
19901

Applicants with the most clearances

Product code EXN
Applicants holding the most 510(k) clearances under product code EXN
ApplicantClearances
Safte S.p.A.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 68 companies shown, in name order