Modern Medical Equipment Manufacturing, Ltd.

FDA Regulatory Profile

Modern Medical Equipment Manufacturing, Ltd. has 0 FDA recalls, 1 inspection, 8 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 21, 2009 · NAI
Latest 510(k)
Mar 17, 2022

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances8Oct 4, 2026Not statedCurrent
Inspections1Oct 23, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 21, 2009Dongguan, ChinaDevicesNo Action Indicated (NAI)3001319476

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

Recent 510(k) Clearances

K-NumberDeviceDate
K210315Single Use Hand Switch Monopolar Forceps with Smoke Evacuation, Single Use Hand Switch Bipolar…Mar 17, 2022
K211170Single Use Irrigation bipolar cableOct 19, 2021
K200372Smoke Evacuation Fingerswitch, Smoke evacuation system with electrosurgical pencilNov 30, 2020
K192542Foot Control Electrosurgical Pencil, Push Button Electrosurgical Pencil, Rocker Switch…Jun 16, 2020
K170703Single Use Arthroscopic Electrode (with Pencil)May 31, 2018
K163442Single Use Micro Electrode (Brass with gold plated shaft); Single Use Micro Electrode (Stainless…Sep 28, 2017
K152059Disposable General ElectrodeApr 21, 2016
K134006DISPOSABLE LAPAROSCOPIC ELECTRODE, DISPOSABLE LAPAROSCOPIC ELECTRODENov 21, 2014