510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K120764Substantially Equivalent

Epiflo(r)

Neogenix, LLC, Beachwood OH / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K120764 is the FDA 510(k) clearance record for EPIFLO(R), a class II device, cleared for Neogenix, LLC on under FDA product code KPJ (Chamber, Oxygen, Topical, Extremity). FDA records list one 510(k) clearance for Neogenix, LLC. As of , FDA records show no recalls naming K120764.

Clearance record

Decision date
Received
(45 days to decision)
Product code
KPJ Chamber, Oxygen, Topical, Extremity
Regulation
21 CFR 878.5650
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Neogenix, LLC 3401 Enterprise Pkwy., Suite 340, Beachwood OH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KPJ

Trailing 12 months

FDA records hold no clearances under product code KPJ in the trailing twelve months.

FDA records show no clearances under product code KPJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260