510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K960388Substantially Equivalent

Dynarex Non-Woven Sponge

Dynarex Corp., Brewster NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960388 is the FDA 510(k) clearance record for DYNAREX NON-WOVEN SPONGE, cleared for Dynarex Corp. on under FDA product code EFQ (Gauze/Sponge, Internal). FDA records list 27 510(k) clearances for Dynarex Corp., from to . As of , FDA records show no recalls naming K960388.

Clearance record

Decision date
Received
(66 days to decision)
Product code
EFQ Gauze/Sponge, Internal
Device class
Unclassified
Review panel
Unknown
Applicant
Dynarex Corp. One International Blvd., Brewster NY
510(k) summary
Statement
Third party review
No

Clearances, product code EFQ

Trailing 12 months

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

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