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Metritrack, Inc.

FDA Regulatory Profile

Metritrack, Inc. has 0 FDA recalls, 2 inspections, 2 510(k) clearances and 0 compliance actions on record.

Latest inspection
Feb 11, 2025 · NAI
Latest 510(k)
May 26, 2021

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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) clearances2Oct 4, 2026Not statedCurrent
Inspections2Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Feb 11, 2025Oak Brook, ILDevicesNo Action Indicated (NAI)3011411309
May 3, 2018Oak Brook, ILDevicesNo Action Indicated (NAI)3011411309

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
K211098Breast Volume Navigator (BVN) Model G-2000May 26, 2021
K141870BREAST VOLUME NAVIGATORAug 7, 2014

FDA data resources