Manufacturer registered with FDA

Arnold Tuber Industries

Orchard Park, NY, United States. Lists 21 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator9059045Contract manufacturerManufacturerRemanufacturerRepacker / relabeler

Device types listed: 21
Brands and models: 23
510(k) clearances: 12009–2009
Markets registered in: 44 registrations outside the US
Establishments: 1United States

510(k) clearances per year, 2000–2026

Registered in 4 markets

Where regulators' registries name Arnold Tuber Industries as the manufacturer or the registration holder of a device.

All markets

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Manufacturer	Arnold Tuber Industries	1 clearances	2009–2009	Below
South Korea	MFDS	Manufacturer	Arnold Tuber Industries	2	2007–2008	Pure Global AI
Costa Rica	Ministerio de Salud	Manufacturer	ARNOLD TUBER INDUSTRIES	1	—	Pure Global AI
Taiwan	TFDA	Manufacturer	Arnold Tuber Industries, LLC.	1	2026–2026	Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Arnold Tuber Industries currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Dental Dressing ForcepsEFL · Class 1	Dental hand instruments	Maker	Forceps	2008
Surgical Tooth Extractor ForcepsEMG · Class 1	Dental hand instruments	Maker	EASY X-TRACForceps	2003
Intraoral Dental DrillDZA · Class 1	Surgical drills & motors	Maker	DENTAL DRILLSDENTAL SCREWS	2003
Dental Surgical Tissue ScissorsEGN · Class 1	Dental hand instruments	Maker	Scissors	2008
Preformed Impression TrayEHY · Class 1	Impression trays	Maker	IMPRESSION TRAYS	2003
All Types RetractorEIG · Class 1	Dental hand instruments	Maker	Retractor	2008
Dental Wax CarverEIK · Class 1	Dental hand instruments	Maker	Carver	2003
Periodontic ProbeEIX · Class 1	Dental hand instruments	Maker	Probe	2003
Cartridge SyringeEJI · Class 2	Dental needles & syringes	Maker	Syringe	2009
Dental BurEJL · Class 1	Dental burs & diamonds	Maker	DENTAL BURS	2003
Endodontic Root Canal PluggerEKR · Class 1	Dental hand instruments	Maker	Plugger	2003
Surgical Rongeur ForcepsEMH · Class 1	Dental hand instruments	Maker	Rongeur	2003
Surgical Bone FileEMI · Class 1	Dental hand instruments	Maker	Bone file	2008
Dental Surgical ElevatorEMJ · Class 1	Dental hand instruments	Maker	Elevator	2003
Dental Surgical CuretteEMK · Class 1	Dental hand instruments	Maker	CURETTE	2003
Surgical Bone ChiselEML · Class 1	Dental hand instruments	Maker	Bone Chisel	2003
Periodontic ScalerEMN · Class 1	Dental hand instruments	Maker	Scaler	2003
Periodontic KnifeEMO · Class 1	Dental hand instruments	Maker	Periodontic Knife	2003
Periodontic HoeEMQ · Class 1	Dental hand instruments	Maker	Hoe	2008
Periodontic FileEMR · Class 1	Dental hand instruments	Maker	Periodontic File	2008
Periodontic CuretteEMS · Class 1	Dental hand instruments	Maker	Curette	2003

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Arnold Tuber Industries as the applicant.

Decided	510(k)	Device	Device type
11 Dec 2009	K092943	ASPIRATING SYRINGE, NON-ASPIRATING SYRINGE	EJI Cartridge Syringe

Some of these clearances are listed with FDA today by another company: Septodont (1).

Also lists devices cleared under other names

Arnold Tuber Industries lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: A. Titan Instruments, Inc. (1).

Decided	510(k)	Device	Applicant	Device type
12 Jun 2006	K060691	EASY X-TRAC SYSTEM	A. Titan Instruments, Inc.	EMG Surgical Tooth Extractor Forceps

Registered establishments

Establishment	Location	What it does
ARNOLD TUBER INDUSTRIESFDA reg. 3003988575	Orchard Park, NY, United States	Contract manufacturer, Manufacturer, Remanufacturer, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9059045). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.