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Data / Medical devices / United States / Elastic Therapy, LLC

Elastic Therapy, LLC: FDA-registered device maker in Asheboro, NC, United States, 1 510(k) clearance

Elastic Therapy, LLC is registered with the FDA (registration 1057079) in Asheboro, NC, United States. It lists 24 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 6, 1993. Registered through 2026. FDA data exported November 2, 2026.

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Get makers like this oneWatch Elastic Therapy, LLC
FDA registration number
1057079
FEI number
1000132035
Address
718 Industrial Park Ave, Asheboro, NC, United States, 27205
Owner or operator
Elastic Therapy LLC (10091310)
Roles
Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer
First device listed
August 19, 2024
Registered through
2026
Brand names listed
DJO, LLC

Devices it lists

DeviceProduct codeClassRoleSource
Bandage, ElasticFQM1Specification developeraccessdata.fda.gov
Belt, Pelvic, TractionHSQ1Specification developeraccessdata.fda.gov
Binder, AbdominalFSD1Specification developeraccessdata.fda.gov
Binder, BreastHEF1Specification developeraccessdata.fda.gov
Binder, ElasticKMO1Specification developeraccessdata.fda.gov
Device, Transfer, Patient, ManualFMR1Specification developeraccessdata.fda.gov
Joint, Ankle, External BraceITW1Contract manufacturer, Manufactureraccessdata.fda.gov
Joint, Elbow, External Limb Component, MechanicalIRD1Contract manufacturer, Manufactureraccessdata.fda.gov
Joint, Knee, External BraceITQ1Contract manufacturer, Manufactureraccessdata.fda.gov
Joint, Shoulder, External Limb ComponentIQQ1Specification developeraccessdata.fda.gov
Orthosis, CervicalIQK1Specification developeraccessdata.fda.gov
Orthosis, Limb BraceIQI1Contract manufacturer, Manufacturer, Specification developeraccessdata.fda.gov
Orthosis, Lumbo-SacralIPY1Specification developeraccessdata.fda.gov
Orthosis, Rib Fracture, SoftIPX1Specification developeraccessdata.fda.gov
Orthosis, Sacroiliac, SoftIPW1Specification developeraccessdata.fda.gov
Protector, Skin PressureFMP1Specification developeraccessdata.fda.gov
Shoe, CastIPG1Specification developeraccessdata.fda.gov
Sling, ArmILI1Specification developeraccessdata.fda.gov
Splint, ClavicleIQJ1Specification developeraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Contract manufacturer, Manufactureraccessdata.fda.gov
Stocking, Medical Support (For General Medical Purposes)FQL1Contract manufacturer, Manufactureraccessdata.fda.gov
Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)DWL2Contract manufacturer, Manufactureraccessdata.fda.gov
Support, HerniaEXN1Specification developeraccessdata.fda.gov
Support, Scrotal, TherapeuticFQJ1Repackager or relabeler, Specification 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 6, 1993K925643RX FIT MEDICAL STOCKINGSDWLSubstantially EquivalentElastic Therapy, Inc.accessdata.fda.gov

Compare with other makers

Updated December 6, 1993. 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.