KGFClass III

Adhesive, Tissue For Aneurysmorrhaphy

Unknown

KGF is the FDA product code for Adhesive, Tissue For Aneurysmorrhaphy, a class III device type. As of 2026-09-10, FDA records hold one 510(k) clearance under this code, the most recent dated 1989-06-01, and no recalls.

Classification record

Product code: KGF
Device name: Adhesive, Tissue For Aneurysmorrhaphy
Device class: Class III
Review panel: Unknown
Submission type: PMA
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 1
Ingested recalls: 0

Clearances, product code KGF

By decision year

1 clearance under product code KGF with a decision year between 1989 and 1989, 1989 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code KGF by decision year
Year	Clearances
1989	1

Applicants with the most clearances

Product code KGF

Applicants holding the most 510(k) clearances under product code KGF
Applicant	Clearances
Medtronic, Inc.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code KGF.

Recent clearances

Product code KGF

K890021Class IIISterile Polyhesive Pbs DressingValleylab, Inc. / cleared 1989-06-01

Recent recalls

Product code KGF

FDA records show no recalls under product code KGF.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)