Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K022043Substantially Equivalent

Smart Plug, Model 500; Smartplug Forceps, Model 502; Push Rod, Model 503

Medennium, Inc., Irvine CA / Traditional, Substantially Equivalent

K022043 is the FDA 510(k) clearance record for SMART PLUG, MODEL 500; SMARTPLUG FORCEPS, MODEL 502; PUSH ROD, MODEL 503, cleared for Medennium, Inc. on under FDA product code LZU (Plug, Punctum). FDA records list one 510(k) clearance for Medennium, Inc. As of , FDA records show no recalls naming K022043.

Clearance record

Decision date
Received
(116 days to decision)
Product code
LZU Plug, Punctum
Device class
Unclassified
Review panel
Unknown
Applicant
Medennium, Inc. 15350 Barranca Pkwy., Irvine CA
510(k) summary
Statement
Third party review
No

Clearances, product code LZU

Trailing 12 months

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

FDA records show no clearances under product code LZU in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LZU, 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