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Data / Medical devices / United States / Spring Health Products, Inc.

Spring Health Products, Inc.: FDA-registered device maker in Norristown, PA, United States, 1 510(k) clearance

Spring Health Products, Inc. is registered with the FDA (registration 2523990) in Norristown, PA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 29, 1999. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2523990
Address
705 GENERAL WASHINGTON AVE. No. 701, Norristown, PA, United States, 19403
Owner or operator
SPRING HEALTH PRODUCTS, INC. (2523990)
Roles
Manufacturer
First device listed
August 15, 2006
Registered through
2026
Brand names listed
Spring Diamonds, The CURE

Devices it lists

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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
September 29, 1999K992728SPRING POWERLITE 2000EBZSubstantially EquivalentSpring Health Products, Inc.accessdata.fda.gov

Compare with other makers

Updated September 29, 1999. 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.