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Data / Medical devices / United States / Trend Medical, LLC

Trend Medical, LLC: FDA-registered device maker in Bethlehem, PA, United States, 1 510(k) clearance

Trend Medical, LLC is registered with the FDA (registration 3012453117) in Bethlehem, PA, United States. It lists 14 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 5, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3012453117
Address
6583 Ruch Rd, Bethlehem, PA, United States, 18017
Owner or operator
Trend Medical, LLC (10051634)
Roles
Repackager or relabeler, Specification developer
First device listed
April 25, 2016
Registered through
2026
Brand names listed
Back Brace, Knee Brace, Lumbar, Trend DynaWrap Intermittent Compression Unit, Trend DynaWrap Intermittent Compression Wrap, Trend Medical, Trend Therapy Pack

Devices it lists

DeviceProduct codeClassRoleSource
Joint, Ankle, External BraceITW1Specification developeraccessdata.fda.gov
Joint, Hip, External BraceITS1Specification developeraccessdata.fda.gov
Joint, Knee, External BraceITQ1Specification developeraccessdata.fda.gov
Joint, Shoulder, External Limb ComponentIQQ1Specification developeraccessdata.fda.gov
Massager, Powered Inflatable TubeIRP2Repackager or relabeleraccessdata.fda.gov
Orthosis, CervicalIQK1Specification developeraccessdata.fda.gov
Orthosis, Limb BraceIQI1Specification developeraccessdata.fda.gov
Orthosis, LumbarIQE1Specification developeraccessdata.fda.gov
Orthosis, Lumbo-SacralIPY1Specification developeraccessdata.fda.gov
Orthosis, ThoracicIPT1Specification developeraccessdata.fda.gov
Pack, Hot Or Cold, ReusableIME1Repackager or relabeler, Specification developeraccessdata.fda.gov
Sling, ArmILI1Specification developeraccessdata.fda.gov
Sling, Arm, Overhead SupportedILE1Specification developeraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Specification developeraccessdata.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
December 5, 2022K222669Cryopush Cold Compression DeviceIRPSubstantially EquivalentChengdu Cryo-Push Medical Technology Co.,Ltdaccessdata.fda.gov

Compare with other makers

Updated December 5, 2022. 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.