Nolato GW BETHEL

FDA Device Registration & Listing · BETHEL, VT, US · Registration 1219536

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
1219536
FEI Number
1219536
Entity Name
Nolato GW BETHEL
City/State/Country
BETHEL, VT, US
Establishment Address
239 PLEASANT ST., BETHEL, VT 05032, 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

Getinge

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGZ Accessories, Catheter General, Plastic Surgery Class 1 878.4200 2022-01-05
PTL Wire, Guide, Catheter, Exempt Cardiovascular Class 2 870.1330 2024-04-04

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
3002949731 Nolato GW Tucson Tucson, AZ, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1219536. Last updated year: 2026. Please use registration number 1219536 when referencing this establishment in official correspondence.
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