510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K162366Substantially Equivalent

Omega VL

Ov World Co., Ltd., Seoul, KR / Traditional, Substantially Equivalent

K162366 is the FDA 510(k) clearance record for Omega VL, a class II device, cleared for Ov World Co., Ltd. on under FDA product code NEW (Suture, Surgical, Absorbable, Polydioxanone). FDA records list one 510(k) clearance for Ov World Co., Ltd. As of , FDA records show no recalls naming K162366.

Clearance record

Decision date
Received
(556 days to decision)
Product code
NEW Suture, Surgical, Absorbable, Polydioxanone
Regulation
21 CFR 878.4840
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Ov World Co., Ltd. (Gasan-Dong, Formatec Bd)A-202,213 205-28, Gasan Digital 1-R, Seoul, KR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NEW

Trailing 12 months
6 clearances under product code NEW in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NEW, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20261
July 20261
August 20261
September 20261
October 20260