Heubach Corporation

FDA Device Registration & Listing · Rockwood, TN, US · Registration 3043044443

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3043044443
FEI Number
3043044443
Entity Name
Heubach Corporation
City/State/Country
Rockwood, TN, US
Establishment Address
200 Cardiff Valley Rd, Rockwood, TN 37854, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Heubach Corporation (Owner Number: 10095098)
Owner / Operator Contact Address
200 Cardiff Valley Rd, Rockwood, TN 37854, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Steep T APX Patient Positioning

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCX Support, Patient Position Anesthesiology Class 1 868.6820 2026-01-23

Official Correspondent

August Eltz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Heubach Corporation
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3043044443. Last updated year: 2026. Please use registration number 3043044443 when referencing this establishment in official correspondence.
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