Nolato GW Tucson

FDA Device Registration & Listing · Tucson, AZ, US · Registration 3002949731

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
3002949731
FEI Number
3002949731
Entity Name
Nolato GW Tucson
City/State/Country
Tucson, AZ, US
Establishment Address
2901 E Valencia Rd, Tucson, AZ 85706, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
GW Plastics, Inc. (Nolato GW) (Owner Number: 10079988)
Owner / Operator Contact Address
2901 E Valencia Rd, Tucson, AZ 85706, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mallinckrodt Group, Inc Optichamber Diamond with Lite touch mask Mallinckrodt Group, Inc Mallinckrodt Group, Inc Mallinckrodt Inc, Liebel Flarsheim Business Mallinckrodt Inc, Liebel Flarsheim Business Mallinckrodt Inc, Liebel Flarsheim Business

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DXT Injector And Syringe, Angiographic Cardiovascular Class 2 870.1650 2021-01-11
NVP Holding Chambers, Direct Patient Interface Anesthesiology Class 2 868.5630 2022-05-23
DXT Injector And Syringe, Angiographic Cardiovascular Class 2 870.1650 2021-01-11
DXT Injector And Syringe, Angiographic Cardiovascular Class 2 870.1650 2021-01-11
DXT Injector And Syringe, Angiographic Cardiovascular Class 2 870.1650 2021-01-06
DXT Injector And Syringe, Angiographic Cardiovascular Class 2 870.1650 2021-01-11
DXT Injector And Syringe, Angiographic Cardiovascular Class 2 870.1650 2021-01-11

Official Correspondent

Todd Crawford

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GW Plastics, Inc. (Nolato GW)
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
1219536 Nolato GW BETHEL BETHEL, VT, US

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0008-2008 Lemaitre Vascular, Inc. 2
CVI OZ Palm Injector, used to perfuse contrast media into vessels for angiographic procedures. Ref : OZ 1035 (Cardiovascular Innovations LLC)
Z-0039-05 Medrad Inc 2
Stellant Syringe Kit. Sterile Disposable Syringe Kits. CT Injector and Accessories. Catalog number SSS-CTP-QFT

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3002949731. Last updated year: 2026. Please use registration number 3002949731 when referencing this establishment in official correspondence.
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