Manufacturer registered with FDA

Spring Health Products, Inc.

Norristown, PA, United States. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator2523990Manufacturer
Device types listed
2
Brands and models
2
510(k) clearances
11999–1999
Markets registered in
338 registrations outside the US
Establishments
1United States
1999: 11990200020102020

510(k) clearances per year, 1990–2026

Registered in 3 markets

Where regulators' registries name Spring Health Products, Inc. as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedEuropean Union: 36 registrationsSouth Korea: 2 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerSpring Health Products, Inc.1 clearances1999–1999Below
European UnionEUDAMEDManufacturerSpring Health Products, Inc.36—Pure Global AI
South KoreaMFDSManufacturerSpring Health Products, Inc.22002–2003Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Spring Health Products, Inc. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Diamond InstrumentDZP · Class 1Dental burs & diamondsMaker
Spring Diamonds
2006
Ultraviolet Activator for PolymerizationEBZ · Class 2Curing lightsMaker
The CURE
2006

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

510(k) clearances

Clearances on which FDA names Spring Health Products, Inc. as the applicant.

Decided510(k)DeviceDevice type
29 Sep 1999K992728SPRING POWERLITE 2000EBZ Ultraviolet Activator for Polymerization

Registered establishments

EstablishmentLocationWhat it does
SPRING HEALTH PRODUCTS, INC.FDA reg. 2523990NORRISTOWN, PA, United StatesManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 2523990). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.