Skip to the page
Get started – free

Data / Medical devices / Stocking, Elastic / United States

FDA-registered makers of Stocking, Elastic in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Stocking, Elastic (product code ILG). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers of this device in the United StatesWatch these makers
Device
Stocking, Elastic
Product code
ILG
Country
United States

Makers of Stocking, Elastic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
62K Solutions, LLCNorth Andover, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Amitofo Inc.Denver, CO, United StatesManufacturer0000api.fda.gov
Braceability, Inc.Cedar Falls, IA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Carolina Narrow Fabric Co.Winston-Salem, NC, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Carolon Co.Rural Hall, NC, United StatesManufacturer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Hartmann Usa Inc.Rock Hill, SC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Hospora IncIrvine, CA, United StatesSpecification developer0000api.fda.gov
Implus Footcare LLCDurham, NC, United StatesSpecification developer0000api.fda.gov
La Pointique International Ltd.Seattle, WA, United StatesSpecification developer0000api.fda.gov
Lymphedivas LLCDalton, MA, United StatesManufacturer0000api.fda.gov
Medi MFG., Inc.Whitsett, NC, United StatesContract manufacturer0000api.fda.gov
Medi Usa, LPWhitsett, NC, United StatesSpecification developer0000api.fda.gov
North Coast Medical, Inc.Morgan Hill, CA, United StatesManufacturer0000api.fda.gov
Oppo Medical, Inc.Seattle, WA, United StatesSpecification developer0000api.fda.gov
Sigvaris, Inc.Peachtree City, GA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Surgical Appliance Industries, Inc.Cincinnati, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Tex-Care MedicalBurlington, NC, United StatesManufacturer0000api.fda.gov
The Marena Group, LLC.Lawrenceville, GA, United StatesManufacturer0000api.fda.gov
Tenacious Holdings IncSaint Paul, MN, United StatesSpecification developer0000api.fda.gov
Thuasne, LLCKansas City, KS, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov

Updated November 2, 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.