Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2249760

FEI Number

3000200590

Entity Name

UNITED PRODUCTS & INSTRUMENTS, INC.

City/State/Country

DAYTON, NJ, US

Establishment Address

182 Ridge Rd Ste E, DAYTON, NJ 08810, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

UNITED PRODUCTS & INSTRUMENTS, INC. (Owner Number: 9043530)

Owner / Operator Contact Address

182 RIDGE RD., UNIT E, Dayton, NJ 08810, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dermascout G300 Series Microscopes M250 Series Microscopes M280 Series Microscopes G500 Series Microscopes Rock It i Centrifuge

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IBJ	Light, Microscope	Pathology	Class 1	864.3600	2009-03-05
GLE	Mixer, Blood Tube	Clinical Chemistry	Class 1	862.2050	2008-11-05
GKG	Centrifuge, Hematocrit	Hematology	Class 2	864.6400	2008-11-05
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	Clinical Chemistry	Class 1	862.2050	2022-03-01

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

UNITED PRODUCTS & INSTRUMENTS, INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2008	Beckman Coulter Inc	1	FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013	Biomerieux Inc	1	PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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3006973688	JIASHAN YINGJIE ELECTRON CO LTD	Jiashan Zhejiang, CN
3032109	Gynex Corporation	North Richland Hills, TX, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2249760. Last updated year: 2026. Please use registration number 2249760 when referencing this establishment in official correspondence.