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Data / Medical devices / United Kingdom / Meridian Technique Ltd

Meridian Technique Ltd: FDA-registered device maker in SOUTHAMPTON Hampshire, United Kingdom, 2 510(k) clearances

Meridian Technique Ltd is registered with the FDA (registration 3004537781) in SOUTHAMPTON Hampshire, United Kingdom. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated October 18, 2017. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3004537781
Address
Epsilon House, Enterprise Road SOUTHAMPTON SCIENCE PARK, SOUTHAMPTON Hampshire, United Kingdom, SO16 7NS
Owner or operator
MERIDIAN TECHNIQUE LTD (9057812)
Roles
Manufacturer
First device listed
December 27, 2007
Registered through
2026
Brand names listed
Orthoview, Orthoview 7.2

Devices it lists

DeviceProduct codeClassRoleSource
System, Image Processing, RadiologicalLLZ2Manufactureraccessdata.fda.gov

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 18, 2017K171068OrthoView 7.2LLZSubstantially EquivalentMeridian Technique, Ltd.accessdata.fda.gov
November 22, 2006K063327ORTHOVIEWLLZSubstantially EquivalentMerdian Technique, Ltd.accessdata.fda.gov

Compare with other makers

Updated October 18, 2017. 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.