UNITED HEALTH PRODUCTS

FDA Device Registration & Listing · Mount Laurel, NJ, US · Registration 3011849720

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
3011849720
FEI Number
3011849720
Entity Name
UNITED HEALTH PRODUCTS
City/State/Country
Mount Laurel, NJ, US
Establishment Address
520 Fellowship Rd Ste 406-D, Mount Laurel, NJ 08054, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
United Health Products (Owner Number: 10054209)
Owner / Operator Contact Address
520 Fellowship Road, Suite 406-D, Mount Laurel, NJ 08054, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Hemostyp Quickseal Hemostyp

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EFN Cotton, Roll Dental Class 1 872.6050 2017-02-23
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2017-02-23
NAB Gauze / Sponge,Nonresorbable For External Use General, Plastic Surgery Class 1 878.4014 2017-02-23

Official Correspondent

Brian Thom

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

United Health Products
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
K843874 Beiersdorf, Inc. LEUKOPOR SURGICAL TAPE 1985-02-21
K915446 Sun Glitz Corp. STRETCH WRAP 1992-05-06
K833120 Acme United Corp. ONE TIME COMPOUND BENZOIN TINCTURE- 1983-12-29
K870091 Avery Intl. IV SECUREMENT DEVICE USING PCCE THERMO. FILM 1987-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011849720. Last updated year: 2026. Please use registration number 3011849720 when referencing this establishment in official correspondence.
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