THE HIBBERT GROUP - Corp Center

FDA Device Registration & Listing · Hamilton, NJ, US · Registration 3001728571

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
3001728571
FEI Number
3001728571
Entity Name
THE HIBBERT GROUP - Corp Center
City/State/Country
Hamilton, NJ, US
Establishment Address
400 Pennington Ave, Hamilton, NJ 08650, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
The Hibbert Group (Owner Number: 10028889)
Owner / Operator Contact Address
400 Pennington Ave, Trenton, NJ 08618, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K212015
PMA Number
N/A

All Registered Proprietary Names

Nano 2nd Gen BD Nano 2nd Gen Pen Needle Nano

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GAA Needle, Aspiration And Injection, Disposable General, Plastic Surgery Class 1 878.4800 2009-03-17
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2025-01-06

Official Correspondent

Michelle Bradley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Hibbert Group
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005676736 THE HIBBERT GROUP - WDC NJ Trenton, NJ, US
3007527549 The Hibbert Group Aurora, CO, US
3007417132 THE HIBBERT GROUP - WDC Delaware New Castle, DE, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K781371 Ferris Mfg. Corp. BONE MARROW ASPIRATION KIT 1978-09-20
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0017-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle and Vacu-lok Aspirating Syringe Catalog Number: 4620
Z-0018-2023 Hobbs Medical, Inc. 1
Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
Z-0023-2011 Becton Dickinson & Company 1
BD 30G1/2 PrecisionGlide Needle;Catalog/Lot Number: 305106. Needles are intended for use in aspiration and injection of medications.
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001728571. Last updated year: 2026. Please use registration number 3001728571 when referencing this establishment in official correspondence.
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