Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2523990

FEI Number

2523990

Entity Name

SPRING HEALTH PRODUCTS, INC.

City/State/Country

NORRISTOWN, PA, US

Establishment Address

705 GENERAL WASHINGTON AVE., No. 701, NORRISTOWN, PA 19403, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SPRING HEALTH PRODUCTS, INC. (Owner Number: 2523990)

Owner / Operator Contact Address

705 GENERAL WASHINGTON AVE., #701, Norristown, PA 19403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

The CURE Spring Diamonds

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EBZ	Activator, Ultraviolet, For Polymerization	Dental	Class 2	872.6070	2006-08-15
DZP	Instrument, Diamond, Dental	Dental	Class 1	872.4535	2006-08-15

Official Correspondent

JOHN TLUSH

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SPRING HEALTH PRODUCTS, INC.

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
K243921	Foshan Coxo Medical Instrument Co., Ltd.	LED Curing Lights (DB686 HALO)	2025-04-11
K033201	Apoza Enterprise Co., Ltd.	LA500 BLUE LIGHT	2003-12-02

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2523990. Last updated year: 2026. Please use registration number 2523990 when referencing this establishment in official correspondence.