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Medrange Corporation

FDA Regulatory Profile

Medrange Corporation has 0 FDA recalls, 3 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 24, 2026 · NAI
Latest 510(k)
Sep 18, 2020

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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) clearances3Oct 4, 2026Not statedCurrent
Inspections3Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 24, 2026Brea, CADevicesNo Action Indicated (NAI)3008786200
Aug 12, 2019Brea, CADevicesNo Action Indicated (NAI)3008786200
Sep 17, 2013Brea, CADevicesVoluntary Action Indicated (VAI)3008786200

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
K201224Electrosurgical Generator and AccessoriesSep 18, 2020
K122092MEDRANGE ELECTROSURGICAL EXPANSION SYSTEMOct 23, 2012
K102114MEDRANGE ELECTROSURGICAL GENERATORNov 22, 2010

FDA data resources