SHELDON MFG., INC.

FDA Device Registration & Listing · CORNELIUS, OR, US · Registration 3024716

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
3024716
FEI Number
3024716
Entity Name
SHELDON MFG., INC.
City/State/Country
CORNELIUS, OR, US
Establishment Address
300 NORTH 26TH AVE., CORNELIUS, OR 97113, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SHELDON MFG., INC. (Owner Number: 3024716)
Owner / Operator Contact Address
300 NORTH 26TH AVE., --, Cornelius, OR 97113, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SHELLAB SHELLAB SHELLAB

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
JRJ Unit, Drying Clinical Chemistry Class 1 862.2050 2009-06-23
JTQ Bath, Incubators/Water, All Microbiology Class 1 866.2540 2001-11-28
JTM Anaerobic Box Glove Microbiology Class 1 866.2120 2009-06-23

Official Correspondent

Roxann Pottratz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SHELDON MFG., INC.
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 3024716. Last updated year: 2026. Please use registration number 3024716 when referencing this establishment in official correspondence.
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