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Advanced Medical Solutions Limited: FDA-registered device maker in PLYMOUTH Devon, United Kingdom, 8 510(k) clearances and 1 PMA approval

Advanced Medical Solutions Limited is registered with the FDA (registration 9617175) in PLYMOUTH Devon, United Kingdom. It lists 5 device types. The FDA files 8 510(k) clearances and 1 PMA approval under its listings, the newest dated June 2, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
9617175
FEI number
3010571423
Address
Western Wood Way Langage Science Park, PLYMOUTH Devon, United Kingdom, PL7 5BG
Owner or operator
ADVANCED MEDICAL SOLUTIONS GROUP PLC (9031453)
Roles
Manufacturer
First device listed
November 20, 2006
Registered through
2026
Brand names listed
Flow Control, Integuseal, LIQUIFIX FIX8, LIQUIFIX Precision, LiquiBand, LiquiBand Butyl, LiquiBand Exceed, LiquiBand Octyl and more

Devices it lists

DeviceProduct codeClassRoleSource
Bandage, LiquidKMF1Manufactureraccessdata.fda.gov
Cutaneous Tissue Adhesive With MeshOMD2Manufactureraccessdata.fda.gov
Sealant, MicrobialNZP2Manufactureraccessdata.fda.gov
Tissue Adhesive For The Topical Approximation Of SkinMPN2Manufactureraccessdata.fda.gov
Tissue Adhesive Internal UsePLJ3Manufactureraccessdata.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
May 23, 2022K211878LiquiBand XLOMDSubstantially EquivalentAdvanced Medical Solutions Limitedaccessdata.fda.gov
March 9, 2020K183570LiquiBand PlusMPNSubstantially EquivalentAdvanced Medical Solutions Limitedaccessdata.fda.gov
October 26, 2015K151182LiquiBand ExceedMPNSubstantially EquivalentAdvanced Medical Solutions (Plymouth), Ltd.accessdata.fda.gov
July 10, 2014K133443MARATHON NO STING LIQUID SKIN PROTECTANTKMFSubstantially EquivalentAdvanced Medical Solutions (Plymouth), Ltd.accessdata.fda.gov
December 20, 2013K132243BARLE TISSUE ADHESIVE 2MPNSubstantially EquivalentAdvanced Medical Solutions (Plymouth), Ltd.accessdata.fda.gov
October 26, 2012K122446LIQUIDBAND FLOW CONTROLMPNSubstantially EquivalentAdvanced Medical Solutions (Plymouth), Ltd.accessdata.fda.gov
February 12, 2009K083531LIQUIBAND ULTIMA, MODEL LB0004MPNSubstantially EquivalentMedlogic Global , Ltd.accessdata.fda.gov
September 29, 2006K052870INTEGUSEAL MICROBIAL SEALANT, MODEL IS 100 AND 1S200NZPSubstantially EquivalentKimberly-Clark Corp.accessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
June 2, 2023P220024LIQUIFIX FIX8 Hernia Mesh Fixation (HMF) Device, LIQUIFIX Precision Open Hernia Mesh Fixation DevicePLJ4October 23, 2026accessdata.fda.gov

Compare with other makers

Updated October 23, 2026. 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.