Data / Medical devices / United States / Neochild, LLC

Neochild, LLC: FDA-registered device maker in Oklahoma City, OK, United States, 7 510(k) clearances

Name: Neochild, LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Neochild, LLC is registered with the FDA (registration 3006271008) in Oklahoma City, OK, United States. It lists 7 device types. The FDA files 7 510(k) clearances under its listings, the newest dated November 22, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3006271008
Address: 413 N Meridian Ave, Oklahoma City, OK, United States, 73107
Owner or operator: NEOCHILD, LLC (9101400)
Roles: Manufacturer, Repackager or relabeler, Specification developer
First device listed: May 9, 2007
Registered through: 2026
Brand names listed: 3.5 Fr. Silicone Urinary Collection Kit with catheter, 5 Fr. Silicone Urinary Collection Kit with catheter, 6.5 Fr. Silicone Urinary Collection Kit with catheter, 8 Fr. Silicone Urinary Collection Kit with catheter, Catherization Tray, Enteral Feeding Tube non-IV adaptor, Enteral Feeding extension sets, Enteral Feeding tube - Polyurethane IV and Non-IV style and more

Devices it lists

Device	Product code	Class	Role	Source
Catheter, Urethral	GBM	2	Manufacturer	accessdata.fda.gov
Enteral Syringes With Enteral Specific Connectors	PNR	2	Repackager or relabeler	accessdata.fda.gov
General Surgery Tray	LRO	2	Specification developer	accessdata.fda.gov
Kit, Surgical Instrument, Disposable	KDD	1	Repackager or relabeler	accessdata.fda.gov
Needle, Conduction, Anesthetic (W/Wo Introducer)	BSP	2	Repackager or relabeler	accessdata.fda.gov
Set, Administration, Intravascular	FPA	2	Specification developer	accessdata.fda.gov
Tubes, Gastrointestinal (And Accessories)	KNT	2	Specification developer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
November 22, 2016	K160855	U&U Enteral Syringe	PNR	Substantially Equivalent	U&U Medical Technology Co, Ltd.	accessdata.fda.gov
December 21, 2012	K120475	ANESTHESIA CONDUCTION NEEDLES	BSP	Substantially Equivalent	Shanghai Samedical & Plastic Instruments Co., Ltd.	accessdata.fda.gov
January 23, 2009	K082710	SAFECHILD ENTERAL FEEDING TUBE AND ACCESSORIES AND FEEDING TUBE EXTENSION SET	KNT	Substantially Equivalent	Neochild, LLC	accessdata.fda.gov
December 19, 2007	K072756	NON-IV ADAPTER FOR INFANT NG TUBE	KNT	Unknown	Promedic, Inc.	accessdata.fda.gov
February 24, 2006	K060268	PEDIATRIC URINARY CATHETER	GBM	Substantially Equivalent	Clay Kennard	accessdata.fda.gov
November 9, 2005	K052903	PEDIATRIC FEEDING TUBE	KNT	Substantially Equivalent	Promedic, Inc.	accessdata.fda.gov
February 5, 2001	K003854	INTRAVASCULAR ADMINISTRATION SET	FPA	Substantially Equivalent	Infusion Devices, Inc.	accessdata.fda.gov

Compare with other makers

Updated November 22, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.