Manufacturer registered with FDA

American Angle Ortho, LLC

Brooklyn, NY, United States. Lists 7 dental device types with FDA across 1 registered establishment.

FDA owner/operator10092173Contract manufacturerSpecification developer
Device types listed
7
Brands and models
10
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1United States

Devices listed with FDA

What American Angle Ortho, LLC currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Orthodontic TubeDZD · Class 1Orthodontic wires & bandsMaker
Buccal Tubes orthodontics
2024
Mouth MirrorEAX · Class 1Dental hand instrumentsMaker
Aurora Stainless Steel Mirrors, Aurora Glass Mirrors
2024
Orthodontic Elastic BandECI · Class 1Orthodontic wires & bandsMaker
Donuts Elastic, Donuts Elastomeric Ligature Ties, Donuts Power Chains,Donuts Rotaition Wedges, Donuts Bumper Tubing, Donuts Separators
2024
Orthodontic Wire ClampECN · Class 1—Maker
Beta Titanium Archwires, Cord Archwire SpringsBrilliance Ceramic Bracket, Pearl Ceramic Bracket, Pearl-Compact Ceramic Brackets,Cord Nickel Titanium Archwires, Cord Stainless Steel Archwires, Cord
2024
Orthodontic Metal BracketEJF · Class 1Orthodontic bracketsMaker
Pro-Master Metal Bracket, Alaska Metal Bracket, Compact-Passive Metal Bracket, Compact-Active Metal Bracket
2024
Orthodontic PlierJEX · Class 1Dental hand instrumentsMaker
Pliers orthodontics
2024
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
AUX Buttons, AUX Hooks, AUX Stops, AUX Golden Chain, AUX Sheath & Cleat,
2024

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

EstablishmentLocationWhat it does
The American Angle, LLCFDA reg. 3034725654Brooklyn, NY, United StatesContract manufacturer, Specification developer

Other names on FDA records

The American Angle, LLC

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10092173). 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.