DELL CORNING CORPORATION

FDA Device Registration & Listing · Spartanburg, SC, US · Registration 3004113569

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
3004113569
FEI Number
3004113569
Entity Name
DELL CORNING CORPORATION
City/State/Country
Spartanburg, SC, US
Establishment Address
575 John Dodd Rd, Spartanburg, SC 29303, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Dell Corning Corporation (Owner Number: 10082321)
Owner / Operator Contact Address
575 John Dodd Rd, Spartanburg, SC 29303, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K230633
PMA Number
N/A

All Registered Proprietary Names

APOLLO ADVANTAGE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LZA Polymer Patient Examination Glove General Hospital Class 1 880.6250 2025-02-12

Official Correspondent

Dawn Bell

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Dell Corning Corporation
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
K212801 Hong Seng Gloves Sdn Bhd Powder free nitrile examination glove- black, non sterile 2022-01-09
K260806 Vista Industries,, LLC Nitrile Disposable Examination Gloves 2026-06-03
K011593 Ansell Healthcare Products, Inc. MICRO-TOUCH NITRILE POWDER FREE SYNTHETIC MEDICAL EXAMINATION GLOVES, COLOR BLUE NON-STERILE 2001-06-21
K981039 Sri Johani Sdn. Bhd. POWDERFREE GREEN NITRILE EXAMINATION GLOVES (POLYMER COATED) 1998-04-21
K101595 Better Care Plastic Technology Cp., Ltd. POWDER FREE NITRILE PATIENT EXAMINATION GLOVES, BLUE 2010-08-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004113569. Last updated year: 2026. Please use registration number 3004113569 when referencing this establishment in official correspondence.
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