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Titan Manufacturing, Inc.

FDA Regulatory Profile

Titan Manufacturing, Inc. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 0 compliance actions on record.

Latest inspection
Aug 9, 2023 · NAI
Latest 510(k)
Oct 25, 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) clearances1Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 9, 2023Fall River, MADevicesNo Action Indicated (NAI)3001452522
Mar 26, 2018Fall River, MADevicesNo Action Indicated (NAI)3001452522

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
K213386Titan Manufacturing Bipolar ForcepsOct 25, 2021

FDA data resources