510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K901340Substantially Equivalent

Model Mc 2100 Nd:yag Surgical Laser System

Klinger Medical, Mission Viejo CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901340 is the FDA 510(k) clearance record for MODEL MC 2100 ND:YAG SURGICAL LASER SYSTEM, a class II device, cleared for Klinger Medical 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 Klinger Medical. As of , FDA records show no recalls naming K901340.

Clearance record

Decision date
Received
(96 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
Klinger Medical 27812 Ruisenor, Mission Viejo CA
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