Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2025917

FEI Number

2025917

Entity Name

NEOTECH PRODUCTS, LLC

City/State/Country

Valencia, CA, US

Establishment Address

28430 Witherspoon Pkwy, Valencia, CA 91355, US

Establishment Type(s)

Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

Neotech Products LLC (Owner Number: 2025917)

Owner / Operator Contact Address

28430 Witherspoon Parkway, --, Valencia, CA 91355, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MECONIUM ASPIRATOR Flow Caddy Neotech ChinStrap Curved Sucker LITTLE SUCKER LITTLE SUCKER WITH COVER SNORKEL SUCTION CADDY NEOLEADS Syringe 20ml / 60ML RAM CANNULA HOLD-A-LINE NEOBRIDGE NEOPULSE NeoGlo Disposable NeoSnug NeoHeart Softsil NeoShape, Heart NeoBond NeoSmile NeoSmile Plus EZ CARE NEOBAR Neotech Bridge NeoGlo and Sleeve NEOSEAL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2007-11-27
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2017-02-13
CCX	Support, Patient Position	Anesthesiology	Class 1	868.6820	2013-02-13
JOL	Catheter And Tip, Suction	General Hospital	Class 2	880.6740	2005-08-30
DRX	Electrode, Electrocardiograph	Cardiovascular	Class 2	870.2360	2007-11-27
PNR	Enteral Syringes With Enteral Specific Connectors	Gastroenterology, Urology	Class 2	876.5980	2023-01-13
CAT	Cannula, Nasal, Oxygen	Anesthesiology	Class 1	868.5340	2011-11-15
KMK	Device, Intravascular Catheter Securement	General Hospital	Class 1	880.5210	2004-09-20
FQM	Bandage, Elastic	General Hospital	Class 1	880.5075	2011-11-15
HJM	Transilluminator, Ac-Powered	Ophthalmic	Class 2	886.1945	2021-04-26
PLI	Gastrointestional Tube Holder	Gastroenterology, Urology	Class 2	876.5980	2023-08-02
DRX	Electrode, Electrocardiograph	Cardiovascular	Class 2	870.2360	2019-05-29
KGX	Tape And Bandage, Adhesive	General Hospital	Class 1	880.5240	2004-09-20
CBH	Device, Fixation, Tracheal Tube	Anesthesiology	Class 1	868.5770	2004-09-20
HGY	Pump, Breast, Non-Powered	Obstetrics/Gynecology	Class 1	884.5150	2022-12-22
HJN	Transilluminator, Battery-Powered	Ophthalmic	Class 1	886.1945	2017-04-19
BXJ	Clip, Nose	Anesthesiology	Class 1	868.6225	2011-11-15

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Neotech Products 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
K934333	3M Medical Products Group	3M RED DOT 2237 STICKY GEL MONITORING ECG ELECTRODE	1994-07-07
K203410	Shantou Wealy Medical Instrument Co.,Ltd	ENFit Disposable Enteral Syringe	2021-06-28
K843874	Beiersdorf, Inc.	LEUKOPOR SURGICAL TAPE	1985-02-21
K915446	Sun Glitz Corp.	STRETCH WRAP	1992-05-06
K833120	Acme United Corp.	ONE TIME COMPOUND BENZOIN TINCTURE-	1983-12-29

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2013	Invuity, Inc.	2	BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a sterilization tray. The Invuity Brite Field Illuminated Suction Device is intended to aspirate from the surgical site and to provide illumination from a high intensity light source.

Similar Registrations

Registration Number	Establishment Name	Location
3016676856	QUICK AID LLC	Clearwater, FL, US
1062154	NDH MEDICAL, INC.	Saint Petersburg, FL, US
3025831202	TKR HUANAN ELECTRONICS (DONGGUAN) CO., LTD.	Dongguan City Guangdong, CN
3011237770	Vygon Verneuil	Verneuil En Halatte Oise, FR
3016734145	CREATE BIOTECH CO., LTD.	Taoyuan City, TW

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2025917. Last updated year: 2026. Please use registration number 2025917 when referencing this establishment in official correspondence.