510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092488Substantially Equivalent

Dynarex Sterile Lubricating Jelly

Dynarex Corp., Orangeburg NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K092488 is the FDA 510(k) clearance record for DYNAREX STERILE LUBRICATING JELLY, a class I device, cleared for Dynarex Corporation on under FDA product code KMJ (Lubricant, Patient). FDA records list 27 510(k) clearances for Dynarex Corporation, from to . As of , FDA records show one recall naming K092488.

Clearance record

Decision date
Received
(127 days to decision)
Product code
KMJ Lubricant, Patient
Regulation
21 CFR 880.6375
Device class
Class I
Review panel
General Hospital
Applicant
Dynarex Corporation 10 Glenshaw St., Orangeburg NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KMJ

Trailing 12 months

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

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