510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K854027Substantially Equivalent

Laserscope Omni Plus Photosurgical System

Laserscope, Santa Clara CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K854027 is the FDA 510(k) clearance record for LASERSCOPE OMNI PLUS PHOTOSURGICAL SYSTEM, a class II device, cleared for Laserscope on under FDA product code LNK (Laser For Gastro-Urology Use). FDA records list 60 510(k) clearances for Laserscope, from to . As of , FDA records show no recalls naming K854027.

Clearance record

Decision date
Received
(62 days to decision)
Product code
LNK Laser For Gastro-Urology Use
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Laserscope 3350 Scott Blvd., Bldg.30, Santa Clara CA
Third party review
No

Clearances, product code LNK

Trailing 12 months

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

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