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MedX Health Corp.: FDA-registered device maker in MISSISSAUGA Ontario, Canada, 7 510(k) clearances

MedX Health Corp. is registered with the FDA (registration 3003725190) in MISSISSAUGA Ontario, Canada. It lists 3 device types. The FDA files 7 510(k) clearances under its listings, the newest dated October 1, 2008. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3003725190
Address
1495 Bonhill Road Unit 1, MISSISSAUGA Ontario, Canada, L5T 1M2
Owner or operator
MedX Health Corp. (9049054)
Roles
Manufacturer
First device listed
March 29, 2002
Registered through
2026
Brand names listed
Lamp, infrared, therapeutic heating, Light based imaging, Powered Light Based Laser Non-Thermal Instrument with Non-Heating Effect For Adjunctive Use in Pain Therapy, amp, infrared, therapeutic heating

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
October 1, 2008K082707MEDX LPT 200 TETHERED LASER & MEDX LPS 200 (ORALASE) PORTABLE LASERILYSubstantially EquivalentMedx Electronics, Inc.accessdata.fda.gov
September 14, 2007K062736SIASCOPE VPSNSubstantially EquivalentAstron Clinica Limitedaccessdata.fda.gov
May 5, 2005K050022MEDX HOMEILYSubstantially EquivalentMedx Electronics, Inc.accessdata.fda.gov
October 3, 2003K032231MEDX1100 CONSOLE & MEDX 100T AND DUOLIGHT LASER ACCESSORIES, MEDX 100 PORTABLE LASERILYSubstantially EquivalentMedx Electronics, Inc.accessdata.fda.gov
March 24, 2003K024310NMA 1052 CONSOLE SYSTEM WITH NMA 100 LASER ACCESSORYNHNSubstantially EquivalentMedx Electronics, Inc.accessdata.fda.gov
September 10, 2002K021985MEDX LCS LASER SERIESNHNSubstantially EquivalentMedx Electronics, Inc.accessdata.fda.gov
July 12, 2002K020017MEDX 1000 SERIESILYSubstantially EquivalentMedx Electronics, Inc.accessdata.fda.gov

Compare with other makers

Updated October 1, 2008. 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.