510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913575Substantially Equivalent

Gauze Packing, Surgical Sterile and Non-Sterile

Keilei Intl., Inc., Dover NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913575 is the FDA 510(k) clearance record for GAUZE PACKING, SURGICAL STERILE AND NON-STERILE, cleared for Keilei Intl., Inc. on under FDA product code FRO (Dressing, Wound, Drug). FDA records list 5 510(k) clearances for Keilei Intl., Inc., from to . As of , FDA records show no recalls naming K913575.

Clearance record

Decision date
Received
(25 days to decision)
Product code
FRO Dressing, Wound, Drug
Device class
Unclassified
Review panel
Unknown
Applicant
Keilei Intl., Inc. Hamilton Business Park 88, Dover NJ
510(k) summary
Statement
Third party review
No

Clearances, product code FRO

Trailing 12 months
19 clearances under product code FRO in the twelve months to October 2026, January 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code FRO, trailing twelve months
MonthClearances
November 20251
December 20251
January 20264
February 20261
March 20263
April 20261
May 20261
June 20263
July 20260
August 20262
September 20262
October 20260