Prince Sterilization Services, LLC

FDA Device Registration & Listing · Fairfield, NJ, US · Registration 3014498612

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
3014498612
FEI Number
3014498612
Entity Name
Prince Sterilization Services, LLC
City/State/Country
Fairfield, NJ, US
Establishment Address
45 Rt 46E Suite 602 and 57 Rt 46E Pine Brook, NJ 07058, 16 Montesano Rd, Fairfield, NJ 07004, US
Establishment Type(s)
Sterilize Medical Device for Another Party (Contract Sterilizer),Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Prince Sterilization Services, LLC (Owner Number: 10057172)
Owner / Operator Contact Address
45 Rt 46E Suite 602 Pine Brook, NJ 07058, 16 Montesano Rd., Fairfield, NJ 07004, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

3D Printed Nasopharyngeal Swab E1-Guide Soft C-29C, NP Swabs SteriKit

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KXF Applicator, Absorbent Tipped, Non-Sterile General Hospital Class 1 880.6025 2020-09-11
KXG Applicator, Absorbent Tipped, Sterile General Hospital Class 1 880.6025 2020-09-11
LXG Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use Clinical Chemistry Class 1 862.2050 2018-03-02

Official Correspondent

Derek Prince

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Prince Sterilization Services, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2008 Beckman Coulter Inc 1
FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013 Biomerieux Inc 1
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014498612. Last updated year: 2026. Please use registration number 3014498612 when referencing this establishment in official correspondence.
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