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

Closure, Wound, Adhesive

21 CFR 878.4018 / General, Plastic Surgery
FDA source (opens on fda.gov)

MGO is the FDA product code for Closure, Wound, Adhesive, a class I device type, regulated under 21 CFR 878.4018. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and 9 recalls.

Classification record

Product code
MGO
Device name
Closure, Wound, Adhesive
Regulation
21 CFR 878.4018
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
9

Clearances, product code MGO

By decision year
1 clearance under product code MGO with a decision year between 1991 and 1991, 1991 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MGO by decision year
YearClearances
19911

Applicants with the most clearances

Product code MGO
Applicants holding the most 510(k) clearances under product code MGO
ApplicantClearances
DeRoyal Industries, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 39 companies shown, in name order