510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930711Substantially Equivalent

Tri*star

Light Technology Systems, Van Nuys CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930711 is the FDA 510(k) clearance record for TRI*STAR, a class II device, cleared for Light Technology Systems on under FDA product code FSS (Light, Surgical, Floor Standing). FDA records list one 510(k) clearance for Light Technology Systems. As of , FDA records show one recall naming K930711.

Clearance record

Decision date
Received
(169 days to decision)
Product code
FSS Light, Surgical, Floor Standing
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Light Technology Systems 16760 Stagg St., #211, Van Nuys CA
510(k) summary
Summary
Third party review
No

Clearances, product code FSS

Trailing 12 months

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

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