510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K130028Substantially Equivalent

Resurfx 1565Nm Laser Module

Lumenis Ltd, Binyamina, IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K130028 is the FDA 510(k) clearance record for RESURFX 1565NM LASER MODULE, a class II device, cleared for Lumenis, Ltd. on under FDA product code ONG (Powered Laser Surgical Instrument With MicrobeamFractional Output). FDA's definition for product code ONG reads: "A LASER (Light Amplification by Stimulated Emission of Radiation) based device having coherence, collimated and typically monochromatic radiation. The laser output is in form of tiny beams in micro range. Typically, indicated to be used in...". FDA records list 83 510(k) clearances for Lumenis, Ltd., from to . As of , FDA records show no recalls naming K130028.

Clearance record

Decision date
Received
(243 days to decision)
Product code
ONG Powered Laser Surgical Instrument With MicrobeamFractional Output
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Lumenis, Ltd. 31 Haavoda St., Binyamina, IL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ONG

Trailing 12 months

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

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