510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K960653Substantially Equivalent

Monocryl (Poliglecaprone 25) Suture, Dyed (Modified)

Ethicon, Inc, Somerville NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K960653 is the FDA 510(k) clearance record for MONOCRYL (POLIGLECAPRONE 25) SUTURE, DYED (MODIFIED), a class II device, cleared for ETHICON, Inc. on under FDA product code GAN (Suture, Absorbable, Synthetic). FDA records list 208 510(k) clearances for ETHICON, Inc., from to . As of , FDA records show 2 recalls naming K960653.

Clearance record

Decision date
Received
(42 days to decision)
Product code
GAN Suture, Absorbable, Synthetic
Regulation
21 CFR 878.4830
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
ETHICON, Inc. Rte. 22 W. P.O. Box 151, Somerville NJ
510(k) summary
Summary
Third party review
No

Clearances, product code GAN

Trailing 12 months

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

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