510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140039Substantially Equivalent

Polycryl

Aurolab, Madurai, Tamilnadu, IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K140039 is the FDA 510(k) clearance record for POLYCRYL, a class II device, cleared for Aurolab on under FDA product code GAM (Suture, Absorbable, Synthetic, Polyglycolic Acid). FDA records list 4 510(k) clearances for Aurolab, from to . As of , FDA records show no recalls naming K140039.

Clearance record

Decision date
Received
(251 days to decision)
Product code
GAM Suture, Absorbable, Synthetic, Polyglycolic Acid
Regulation
21 CFR 878.4493
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Aurolab No 1, Sivagangai Main Rd., Madurai, Tamilnadu, IN
510(k) summary
Statement
Third party review
No

Clearances, product code GAM

Trailing 12 months
5 clearances under product code GAM in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code GAM, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20261
March 20260
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260