Top Safety Products, Inc.

FDA Device Registration & Listing · Branchburg, NJ, US · Registration 3001106688

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
3001106688
FEI Number
3001106688
Entity Name
Top Safety Products, Inc.
City/State/Country
Branchburg, NJ, US
Establishment Address
160 Meister Ave Ste 16, Branchburg, NJ 08876, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Top Safety Products Company Inc. (Owner Number: 10031457)
Owner / Operator Contact Address
160 Meister Ave, Suite 16, Branchburg, NJ 08876, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Dynarex, MedLine, Moore Medical Eyes Plus, OcuFresh Dynarex, MedLine Zulco, Dynarex Top Safety Product First Aid Kit Top Safety Products

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2010-02-01
JCE Solution, Isotonic Pathology Class 1 864.4010 2015-12-16
BYP Mouthpiece, Breathing Anesthesiology Class 1 868.5620 2013-01-30
LKB Pad, Alcohol, Device Disinfectant Unknown Class U N/A 2015-12-16
JOK Scissors, Medical, Disposable General Hospital Class 1 880.6820 2015-12-16
LRR First Aid Kit With Drug Unknown Class N N/A 2010-02-04
KGB Mask, Oxygen, Non-Rebreathing Anesthesiology Class 1 868.5570 2010-02-01

Official Correspondent

Jennifer Johnson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Top Safety Products Company Inc.
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 3001106688. Last updated year: 2026. Please use registration number 3001106688 when referencing this establishment in official correspondence.
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