Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018056766

FEI Number

3018056766

Entity Name

Celestica DBA ABELCONN, LLC

City/State/Country

Maple Grove, MN, US

Establishment Address

10950 85th Ave N, Suite A, Maple Grove, MN 55369, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Celestica dbs AbelConn, LLC (Owner Number: 10088596)

Owner / Operator Contact Address

10950 85th Ave N, Suite A, Maple Grove, MN 55369, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Podimetrics SmartMat (Model: PMHS201U) Remanufactured Mat 2 assembly (Model: PMHS201U-R)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OIZ	Foot Examination Tool For Inflammatory Changes	Physical Medicine	Class 1	890.5050	2023-08-24

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Celestica dbs AbelConn, LLC

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 3018056766. Last updated year: 2026. Please use registration number 3018056766 when referencing this establishment in official correspondence.