EVCO Plastics-AMP

FDA Device Registration & Listing · Deforest, WI, US · Registration 3009590187

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
3009590187
FEI Number
3009590187
Entity Name
EVCO Plastics-AMP
City/State/Country
Deforest, WI, US
Establishment Address
110 Evco Cir, Deforest, WI 53532, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
DON EVANS, INC. (Owner Number: 2124274)
Owner / Operator Contact Address
121 Evco Circle, --, Deforest, WI 53532, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Welch Allyn Single-Use Ear Specula

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ERA Otoscope Ear, Nose, Throat Class 1 874.4770 2025-04-22

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DON EVANS, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2124274 EVCO PLASTICS, DIV. DON EVANS, INC. DEFOREST, WI, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K932506 Rudolf Riester GmbH & Co. KG RI-SCOPE (S) 1993-10-08

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009590187. Last updated year: 2026. Please use registration number 3009590187 when referencing this establishment in official correspondence.
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