Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K134006Substantially Equivalent

Disposable Laparoscopic Electrode, Disposable Laparoscopic Electrode

Modern Medical Equipment Manufacturing Ltd., Hong Kong, CN / Traditional, Substantially Equivalent

K134006 is the FDA 510(k) clearance record for DISPOSABLE LAPAROSCOPIC ELECTRODE, DISPOSABLE LAPAROSCOPIC ELECTRODE, a class II device, cleared for Modern Medical Equipment Manufacturing Limited on under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories). FDA's definition for product code GEI reads: "Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available...". FDA records list 8 510(k) clearances for Modern Medical Equipment Manufacturing Limited, from to . As of , FDA records show no recalls naming K134006.

Clearance record

Decision date
Received
(329 days to decision)
Product code
GEI Electrosurgical, Cutting & Coagulation & Accessories
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Modern Medical Equipment Manufacturing Limited 35-41 Tai Lin Pai Rd., 5f Gold King Industrial Bldg., Hong Kong, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GEI

Trailing 12 months
47 clearances under product code GEI in the twelve months to October 2026, June 2026 the highest month at 9.
Show the numbers
Monthly 510(k) clearances under FDA product code GEI, trailing twelve months
MonthClearances
November 20254
December 20251
January 20266
February 20263
March 20265
April 20265
May 20264
June 20269
July 20263
August 20262
September 20265
October 20260