405 PLASTICS & DISTRIBUTION, INC

FDA Device Registration & Listing · Oklahoma City, OK, US · Registration 3013545067

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
3013545067
FEI Number
3013545067
Entity Name
405 PLASTICS & DISTRIBUTION, INC
City/State/Country
Oklahoma City, OK, US
Establishment Address
3201 N. Santa Fe, Oklahoma City, OK 73118, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
405 Plastics & Distribution, Inc (Owner Number: 10054676)
Owner / Operator Contact Address
3201 N. Santa Fe, Oklahoma City, OK 73118, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

JumboJug Large Volume Suction Canister

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KDQ Bottle, Collection, Vacuum General Hospital Class 2 880.6740 2017-04-13

Official Correspondent

Richard Clements

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

405 Plastics & Distribution, 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 3013545067. Last updated year: 2026. Please use registration number 3013545067 when referencing this establishment in official correspondence.
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