PHILLIPS SAFETY PRODUCTS, INC.

FDA Device Registration & Listing · Middlesex, NJ, US · Registration 3004183518

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
3004183518
FEI Number
3004183518
Entity Name
PHILLIPS SAFETY PRODUCTS, INC.
City/State/Country
Middlesex, NJ, US
Establishment Address
123 Lincoln Blvd., Middlesex, NJ 08846, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Phillips Safety Products, Inc. (Owner Number: 10026015)
Owner / Operator Contact Address
123 Lincoln Blvd., Middlesex, NJ 08846, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Phillips Safety Products Phillips Safety Products Rubber Restraint Strap Phillips Safety Products Phillips Safety Products Phillips Safety Products Phillips Safety Products

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IWX Barrier, Control Panel, X-Ray, Movable Radiology Class 1 892.6500 2008-05-30
FMQ Restraint, Protective General Hospital Class 1 880.6760 2023-02-02
EAJ Apron, Leaded Radiology Class 1 892.6500 2015-05-11
EAK Screen, Leaded, Operator Radiation Protector Radiology Class 1 892.6500 2015-05-11
IWS Shield, Eye, Radiological Radiology Class 1 892.6500 2015-05-11
HOY Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) Ophthalmic Class 1 886.4750 2015-05-11

Official Correspondent

Robert Phillips

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Phillips Safety Products, 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
K962327 Sekure Seat Corp. SEKURE SEAT ADULT PASSIVE RESTRAINING DEVICE 1997-03-06
K963243 Heelbo, Inc. HEELBO BLAZER SLEEVED JACKET 1996-10-01

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004183518. Last updated year: 2026. Please use registration number 3004183518 when referencing this establishment in official correspondence.
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