Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042641209

FEI Number

3042641209

Entity Name

ANGELALIGN MANUFACTURING CORP.

City/State/Country

Oak Creek, WI, US

Establishment Address

10551 S Oakview Pkwy, Oak Creek, WI 53154, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

ANGELALIGN MANUFACTURING CORP. (Owner Number: 10094928)

Owner / Operator Contact Address

10551 South Oakview Parkway, Oak Creek, WI 53154, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DYT	Maintainer, Space Preformed, Orthodontic	Dental	Class 1	872.5525	2026-01-07

Official Correspondent

Angela Wu

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ANGELALIGN MANUFACTURING CORP.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042641209. Last updated year: 2026. Please use registration number 3042641209 when referencing this establishment in official correspondence.