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Rex Implants, Inc.

FDA Regulatory Profile

Rex Implants, Inc. has 0 FDA recalls, 1 inspection, 1 510(k) clearance and 1 compliance action on record.

Latest inspection
Dec 14, 2023 · OAI
Latest 510(k)
Oct 12, 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) clearances1Oct 4, 2026Not statedCurrent
Inspections1Oct 25, 2026Not statedCurrent
Compliance actions1Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 14, 2023Columbus, OHDevicesOfficial Action Indicated (OAI)3014174860

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
K211872PiezoImplant SystemOct 12, 2022

FDA data resources