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Data / Medical devices / United States / A. Titan Instruments, Inc.

A. Titan Instruments, Inc.: FDA-registered device maker in Orchard Park, NY, United States, 2 510(k) clearances

A. Titan Instruments, Inc. is registered with the FDA (registration 2531684) in Orchard Park, NY, United States. It lists 19 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 12, 2006. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this oneWatch A. Titan Instruments, Inc.
FDA registration number
2531684
FEI number
3002681225
Address
10 Centre Dr, Orchard Park, NY, United States, 14127
Owner or operator
A. TITAN INSTRUMENTS, INC. (9035364)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler
First device listed
April 15, 2002
Registered through
2026
Brand names listed
A. TITAN INSTRUMENTS, A. Titan, Amalgam carrier, Bit 1, Carver, Curette, Easy X-Trac System, Elevator and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessories, Implant, Dental, EndosseousNDP1Repackager or relabeleraccessdata.fda.gov
Accessories, Retractor, DentalEIF1Repackager or relabeleraccessdata.fda.gov
Adaptor, Holder, SyringeIQG1Repackager or relabeleraccessdata.fda.gov
Bur, DentalEJL1Repackager or relabeleraccessdata.fda.gov
Carrier, Amalgam, OperativeEKI1Contract manufacturer, Manufactureraccessdata.fda.gov
Carver, Dental Amalgam, OperativeEKH1Repackager or relabeleraccessdata.fda.gov
Carver, Wax, DentalEIK1Repackager or relabeleraccessdata.fda.gov
Culture Media, Single Biochemical TestJSF1Repackager or relabeleraccessdata.fda.gov
Curette, Surgical, DentalEMK1Repackager or relabeleraccessdata.fda.gov
Elevator, Surgical, DentalEMJ1Repackager or relabeleraccessdata.fda.gov
Excavator, Dental, OperativeEKC1Repackager or relabeleraccessdata.fda.gov
Forceps, Dressing, DentalEFL1Repackager or relabeleraccessdata.fda.gov
Forceps, Tooth Extractor, SurgicalEMG1Repackager or relabeleraccessdata.fda.gov
Gauge, Depth, Instrument, DentalEIL1Repackager or relabeleraccessdata.fda.gov
Handle, Instrument, DentalEJB1Repackager or relabeleraccessdata.fda.gov
Instrument, Filling, Plastic, DentalEIY1Repackager or relabeleraccessdata.fda.gov
Instruments, Dental HandDZN1Repackager or relabeleraccessdata.fda.gov
Kit, Surgical Instrument, DisposableKDD1Repackager or relabeleraccessdata.fda.gov
Scissors, Surgical Tissue, DentalEGN1Repackager or relabeleraccessdata.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
June 12, 2006K060691EASY X-TRAC SYSTEMEMGSubstantially EquivalentA. Titan Instruments, Inc.accessdata.fda.gov
August 20, 1980K801886BURR, DENTALEJLSubstantially EquivalentAesculap Instruments Corp.accessdata.fda.gov

Compare with other makers

Updated June 12, 2006. 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.