Evans Manufacturing

FDA Device Registration & Listing · Garden Grove, CA, US · Registration 1000340275

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
1000340275
FEI Number
1000340275
Entity Name
Evans Manufacturing
City/State/Country
Garden Grove, CA, US
Establishment Address
7422 Chapman Ave., Garden Grove, CA 92841, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Evans Manufacturing LLC (Owner Number: 10037367)
Owner / Operator Contact Address
7422 Chapman Ave., Garden Grove, CA 92841, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Evans Soothe-It Ice/Heat Pack AM/PM Med Minder Med Minder Evans Evans Evans Manufacturing Inc Evans Manufacturing Inc

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 2020-08-05
IME Pack, Hot Or Cold, Reusable Physical Medicine Class 1 890.5700 2024-03-28
NXB Dispenser, Solid Medication Physical Medicine Class 1 890.5050 2024-03-28
HQY Sunglasses (Non-Prescription Including Photosensitive) Ophthalmic Class 1 886.5850 2012-05-14
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2020-07-27
OHO First Aid Kit Without Drug General, Plastic Surgery Class 1 878.4014 2020-07-27
OHY Pill Crusher/Cutter General Hospital Class 1 880.6430 2020-11-04
KYX Dispenser, Liquid Medication General Hospital Class 1 880.6430 2020-09-08

Official Correspondent

John McMahon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Evans Manufacturing LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K944481 Garan Scientific, Inc. THE HEART PROTECTOR 1995-04-10
K940726 Jay-Y Enterprises Co., Inc. NONE-GENERIC 1994-04-11
K934837 Simon Marketing, Inc. SUNGLASSES 1993-12-08
K852902 Yours Enterprise Co., Ltd. METALLIC SUNGLASSES 1985-08-12
K970895 Custom Optical Frames, Inc. CUSTOM OPTICAL SUNGLASS FRAMES 1997-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000340275. Last updated year: 2026. Please use registration number 1000340275 when referencing this establishment in official correspondence.
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