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Data / Medical devices / United States / Arnold Tuber Industries

Arnold Tuber Industries: FDA-registered device maker in Orchard Park, NY, United States, 1 510(k) clearance

Arnold Tuber Industries is registered with the FDA (registration 3003988575) in Orchard Park, NY, United States. It lists 29 device types. The FDA files 1 510(k) clearance 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 Arnold Tuber Industries
FDA registration number
3003988575
Address
10 Centre Dr, Orchard Park, NY, United States, 14127
Owner or operator
ARNOLD TUBER INDUSTRIES (9059045)
Roles
Contract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer
First device listed
October 8, 2003
Registered through
2026
Brand names listed
Bone Chisel, Bone file, CURETTE, Carver, Curette, DENTAL BURS, DENTAL DRILLS, DENTAL SCREWS and more

Devices it lists

DeviceProduct codeClassRoleSource
Bit, DrillHTW1Repackager or relabeler, Specification developeraccessdata.fda.gov
Bur, DentalEJL1Manufactureraccessdata.fda.gov
Carver, Wax, DentalEIK1Manufactureraccessdata.fda.gov
Chisel, Bone, SurgicalEML1Manufactureraccessdata.fda.gov
Curette, PeriodonticEMS1Manufactureraccessdata.fda.gov
Curette, Surgical, DentalEMK1Manufactureraccessdata.fda.gov
Drill, Dental, IntraoralDZA1Manufactureraccessdata.fda.gov
Elevator, Surgical, DentalEMJ1Manufactureraccessdata.fda.gov
Elevator, Surgical, General & Plastic SurgeryGEG1Manufacturer, Remanufacturer, Repackager or relabeleraccessdata.fda.gov
File, Bone, SurgicalEMI1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
File, PeriodonticEMR1Manufactureraccessdata.fda.gov
Forceps, Dressing, DentalEFL1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Forceps, Rongeur, SurgicalEMH1Manufactureraccessdata.fda.gov
Forceps, Tooth Extractor, SurgicalEMG1Manufactureraccessdata.fda.gov
Gag, MouthKBN1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Hoe, PeriodonticEMQ1Manufactureraccessdata.fda.gov
Instrument, Manual, Surgical, General UseMDM1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Instruments, Surgical, CardiovascularDWS1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Knife, PeriodonticEMO1Manufactureraccessdata.fda.gov
Plugger, Root Canal, EndodonticEKR1Manufactureraccessdata.fda.gov
Probe, PeriodonticEIX1Manufactureraccessdata.fda.gov
Retractor, All TypesEIG1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Scaler, PeriodonticEMN1Manufactureraccessdata.fda.gov
Scissors, OphthalmicHNF1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Scissors, Orthopedic, SurgicalHRR1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Scissors, Surgical Tissue, DentalEGN1Remanufacturer, Repackager or relabeleraccessdata.fda.gov
Syringe, CartridgeEJI2Contract manufactureraccessdata.fda.gov
Tray, Impression, PreformedEHY1Manufactureraccessdata.fda.gov
Tray, Surgical, InstrumentFSM1Manufacturer, Remanufacturer, Repackager 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

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.