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Data / Medical devices / United States / Titan Manufacturing Inc.

Titan Manufacturing Inc.: FDA-registered device maker in Fall River, MA, United States, 1 510(k) clearance

Titan Manufacturing Inc. is registered with the FDA (registration 2531415) in Fall River, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 25, 2021. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2531415
FEI number
3001452522
Address
818 Jefferson St, Fall River, MA, United States, 02721
Owner or operator
TITAN MANUFACTURING INC (9025545)
Roles
Complaint file establishment, Manufacturer
First device listed
October 26, 2021
Registered through
2026
Brand names listed
Titan Manufacturing Bipolar Forceps

Devices it lists

DeviceProduct codeClassRoleSource
Electrosurgical, Cutting & Coagulation & AccessoriesGEI2Complaint file establishment, Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
October 25, 2021K213386Titan Manufacturing Bipolar ForcepsGEISubstantially EquivalentTitan Manufacturing, Inc.accessdata.fda.gov

Compare with other makers

Updated October 25, 2021. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.