Manufacturer registered with FDA

Nomax Inc.

Saint Louis, MO, United States. Lists 3 dental device types with FDA across 1 registered establishment.

FDA owner/operator1937310Contract manufacturerRepacker / relabeler

Device types listed: 3
Brands and models: 4
510(k) clearances: 0as applicant
Markets registered in: 21 registrations outside the US
Establishments: 1United States

Registered in 2 markets

Where regulators' registries name Nomax Inc. as the manufacturer or the registration holder of a device.

RegisteredHome: United StatesOne marker per market

Market	Regulator	Named as	Name on the registry	Registrations	Issued	Records
United States	FDA	Manufacturer	Nomax Inc.	3 device types	—	Below
Israel	AMAR	Manufacturer	Nomax Inc.	1	—	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 Nomax Inc. 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 Surgical Tissue ScissorsEGN · Class 1	Dental hand instruments	Lister	Spencer Stitch Scissors 3.5"Vannas Scissors, Curved, Spring HandleVannas Scissors, Straight, Spring Handle	2016
Oral Cavity Abrasive Polishing AgentEJR · Class 1	Polishing & prophylaxis	Maker	PRO CARE PROPHYLAXIS PASTE MIX	1992
Plaque Disclosing KitNYH · Class 2	—	Maker	—	2012

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

Registered establishments

Establishment	Location	What it does
NOMAX, INC.FDA reg. 1937310	Affton, MO, United States	Contract manufacturer, Repacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 1937310). 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.