Product code KGN— Unknown

PRIMATRIX DERMAL REPAIR SCAFFOLD

Classification name
Wound Dressing With Animal-Derived Material(S)
Device class
Unclassified
Advisory panel
Unknown
Total cleared
192
First cleared
Most recent

Market context for product code KGN

FDA has cleared 192 devices under product code KGN between 1979 and 2026, filed by 101 applicant companies. No FDA device recalls reference this product code.

Clearances per year

last 15 years

Top applicants under product code KGN

Adverse events under product code KGN

product code KGN
Other
2
Total
2

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code KGN

1–100 of 192

Data sourced from openFDA. This site is unofficial and independent of the FDA.