Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042028951

FEI Number

3042028951

Entity Name

ABCORP 3D

City/State/Country

Columbia, TN, US

Establishment Address

711 Armstrong Ln, Columbia, TN 38401, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

ABCorp 3D (Owner Number: 10083679)

Owner / Operator Contact Address

225 Rivermoor St, Boston, MA 02132, 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
MVA	Orthosis, Cranial	Neurology	Class 2	882.5970	2024-11-19
OAN	Orthosis, Cranial, Laser Scan	Neurology	Class 2	882.5970	2024-11-19

Official Correspondent

Neil Glazebrook Glazebrook

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ABCorp 3D

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1215709	ABCORP	Boston, MA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042028951. Last updated year: 2026. Please use registration number 3042028951 when referencing this establishment in official correspondence.