510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K952682Substantially Equivalent

Lokki Dt

Lokki, Vienne, FR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952682 is the FDA 510(k) clearance record for LOKKI DT, a class II device, cleared for Lokki on under FDA product code GEX (Powered Laser Surgical Instrument). FDA's definition for product code GEX reads: "A laser (light amplification by stimulated emission of radiation) based device having coherence, collimated and typically monochromatic radiation. Typically indicated to to cut, destroy, remove or coagulate tissue, generally soft tissue...". FDA records list one 510(k) clearance for Lokki. As of , FDA records show no recalls naming K952682.

Clearance record

Decision date
Received
(155 days to decision)
Product code
GEX Powered Laser Surgical Instrument
Regulation
21 CFR 878.4810
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Lokki Pl. Pierre Semard, Vienne, FR
510(k) summary
Statement
Third party review
No

Clearances, product code GEX

Trailing 12 months
70 clearances under product code GEX in the twelve months to October 2026, November 2025 the highest month at 11.
Show the numbers
Monthly 510(k) clearances under FDA product code GEX, trailing twelve months
MonthClearances
November 202511
December 20255
January 20264
February 20266
March 20267
April 20265
May 20268
June 20263
July 20264
August 20264
September 202611
October 20262