PRIMEX DESIGN & FABRICATION

FDA Device Registration & Listing · Richmond, IN, US · Registration 3016871880

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
3016871880
FEI Number
3016871880
Entity Name
PRIMEX DESIGN & FABRICATION
City/State/Country
Richmond, IN, US
Establishment Address
400 Industrial Parkway, Richmond, IN 47374, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Primex Design & Fabrication (Owner Number: 10073902)
Owner / Operator Contact Address
400 Industrial Parkway, Richmond, IN 47374, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Primex Protect

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYU Accessory, Surgical Apparel General, Plastic Surgery Class 1 878.4040 2020-05-15

Official Correspondent

Todd Gray

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Primex Design & Fabrication
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 3016871880. Last updated year: 2026. Please use registration number 3016871880 when referencing this establishment in official correspondence.
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