NEO MEDICAL INC.

FDA Device Registration & Listing · Sparks, NV, US · Registration 3007207906

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
3007207906
FEI Number
3007207906
Entity Name
NEO MEDICAL INC.
City/State/Country
Sparks, NV, US
Establishment Address
249 Freeport Blvd, Sparks, NV 89431, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device
Owner / Operator
Neo Medical Inc. (Owner Number: 10025226)
Owner / Operator Contact Address
249 Freeport Blvd., Sparks, NV 89431, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K863819
PMA Number
N/A

All Registered Proprietary Names

Vascular Port Infusion Needles Neo-Magic & V-Cath PICCs Neo Magic & V-Cath Seldinger and Modified Seldinger Kits Catheter Introducer Needle Sharps Safety Over The Needle Catheters & Introducers Centrasil Central Venous Catheter Silcath Neuro Trace Nerve Locator Poly PICC V-cath & Neo-Magic Sharps Safety Seldinger Needle Pandin Continous Nerve Catheter V-Cath & Neo-Magic Safety OTN C Port PowerStick Power V-Cath Trocar Tunneler Intraperitoneal Catheter

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2011-11-30
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital Class 2 880.5200 2011-11-30
KZH Introducer, Syringe Needle General Hospital Class 2 880.6920 2011-11-30
KZH Introducer, Syringe Needle General Hospital Class 2 880.6920 2011-11-30
DYB Introducer, Catheter Cardiovascular Class 2 870.1340 2011-11-30
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital Class 2 880.5200 2011-11-30
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital Class 2 880.5200 2011-11-30
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days General Hospital Class 2 880.5970 2011-11-30
ETN Stimulator, Nerve Ear, Nose, Throat Class 2 874.1820 2011-11-30
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital Class 2 880.5200 2011-11-30
DYB Introducer, Catheter Cardiovascular Class 2 870.1340 2011-11-30
CAZ Anesthesia Conduction Kit Anesthesiology Class 2 868.5140 2011-11-30
DQY Catheter, Percutaneous Cardiovascular Class 2 870.1250 2011-11-30
DYB Introducer, Catheter Cardiovascular Class 2 870.1340 2011-11-30
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2011-11-30
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days General Hospital Class 2 880.5970 2011-11-30
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days General Hospital Class 2 880.5970 2011-11-30
FJS Catheter, Peritoneal, Long-Term Indwelling Gastroenterology, Urology Class 2 876.5630 2011-11-30

Official Correspondent

Cheryl Brown

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Neo Medical Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3031823165 NEO MEDICAL USA, INC. San Jose, CA, US

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09
K943349 Quinton, Inc. MAHURKAR DUAL LUMEN CATHETER 1995-03-22
K912158 Medical Device Inspection Co., Inc. CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY 1991-10-23
K101883 St Jude Medical 6F ENGAGE/ENGAGE TR INTRODUCER 2010-09-07
K034025 Nmt Medical, Inc. NMT MEDICAL TRANSSEPTAL SHEATH SET, MODELS TSS-10-HSC, TSS-11-HSC, TSS12-HSC 2004-03-26

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
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
Z-0002-2024 ARROW INTERNATIONAL Inc. 2
Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Z-0003-2024 ARROW INTERNATIONAL Inc. 2
Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Z-0009-2023 B Braun Medical Inc 2
Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.
Z-0025-2024 Becton Dickinson Infusion Therapy Systems Inc. 2
REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx Only, Sterile EO

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007207906. Last updated year: 2026. Please use registration number 3007207906 when referencing this establishment in official correspondence.
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