Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006271008

FEI Number

3006271008

Entity Name

NEOCHILD, LLC

City/State/Country

OKLAHOMA CITY, OK, US

Establishment Address

413 N Meridian Ave, OKLAHOMA CITY, OK 73107, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

NEOCHILD, LLC (Owner Number: 9101400)

Owner / Operator Contact Address

413 N Meridian Ave, Oklahoma City, OK 73107, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K072756

PMA Number

N/A

All Registered Proprietary Names

IV extension sets Catherization Tray NC401500 NC401000 NeoChild Enteral Syringes 8 Fr. Silicone Urinary Collection Kit with catheter Lumbar Puncture Tray w/ 22ga, 1.5" Needle 6.5 Fr. Silicone Urinary Collection Kit with catheter 5 Fr. Silicone Urinary Collection Kit with catheter Urinary Collection Kit - No Catheter Lumbar Puncture Tray w/ 22ga, 1" Needle 3.5 Fr. Silicone Urinary Collection Kit with catheter PICC Insertion Tray - No Catheter Umbilical Tray Lumbar Puncture Needles INFANT FEEDING TUBE Infant feeding tubes - PVC IV and non-IV style Enteral Feeding Tube non-IV adaptor

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPA	Set, Administration, Intravascular	General Hospital	Class 2	880.5440	2008-10-31
KDD	Kit, Surgical Instrument, Disposable	General, Plastic Surgery	Class 1	878.4800	2016-03-25
PNR	Enteral Syringes With Enteral Specific Connectors	Gastroenterology, Urology	Class 2	876.5980	2026-02-09
LRO	General Surgery Tray	General, Plastic Surgery	Class 2	878.4370	2016-03-28
BSP	Needle, Conduction, Anesthetic (W/Wo Introducer)	Anesthesiology	Class 2	868.5150	2022-03-06
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2007-05-09
KNT	Tubes, Gastrointestinal (And Accessories)	Gastroenterology, Urology	Class 2	876.5980	2011-12-13

Official Correspondent

Chad Kennard

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NEOCHILD, LLC

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
K221518	Np Medical	NP Medical nCompass Extension Set with Stabilizing Base	2022-11-03
K953474	Medikmark, Inc.	IV START KIT	1995-10-02
K972493	Nipro Medical Corp.	NIPRO DISPOSABLE SOLUTION INFUSION SET	1997-09-18
K982672	Baxter Healthcare Corp	COLLEAGUE PUMP SYRINGE ADAPTER SET	1998-09-04
K143446	Roche Diagnostics GmbH	Accu-Chek FlexLink Plus infusion set	2015-08-13

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0010-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24
Z-0011-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24
Z-0012-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set with 150 mL Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.
Z-0012-2025	Smiths Medical ASD Inc.	2	CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24
Z-0013-2013	Baxter Healthcare Corp. Rt.	2	Baxter Interlink System Buretrol Solution Set, 117" (3.0 m), with 150 mL Burette (Ball-Valve Drip Chamber) (Non-DEHP); a sterile Rx IV fluid pathway device; Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.

Similar Registrations

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1047843	ISOMEDIX OPERATIONS INC.	SPARTANBURG, SC, US
3002807090	Sterigenics Germany GmbH	Wiesbaden Hesse, DE
3013319212	ICU MEDICAL, INC.	Lake Forest, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006271008. Last updated year: 2026. Please use registration number 3006271008 when referencing this establishment in official correspondence.