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Data / Medical devices / United States / Links Medical Products, Inc.

Links Medical Products, Inc.: FDA-registered device maker in Irvine, CA, United States, 1 510(k) clearance

Links Medical Products, Inc. is registered with the FDA (registration 2031987) in Irvine, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 14, 2014. Registered through 2026. FDA data exported November 3, 2026.

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FDA registration number
2031987
FEI number
3002995416
Address
9247 Research Dr, Irvine, CA, United States, 92618
Owner or operator
LINKS MEDICAL PRODUCTS, INC. (9040995)
Roles
Manufacturer
First device listed
May 14, 2014
Registered through
2026

Devices it lists

DeviceProduct codeClassRoleSource
Dressing, Wound, DrugFROUManufactureraccessdata.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
March 14, 2014K131796MANUKA FILL WOUND DRESSINGFROSubstantially EquivalentLinks Medical Products, Inc.accessdata.fda.gov

Compare with other makers

Updated March 14, 2014. 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.