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Data / Medical devices / Binder, Abdominal / United States

FDA-registered makers of Binder, Abdominal in the United States: 31 establishments

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

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Device
Binder, Abdominal
Product code
FSD
Country
United States

Makers of Binder, Abdominal in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3M CompanySaint Paul, MN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Action PackagingWoodstock, IL, United StatesSpecification developer0000api.fda.gov
Bird & Cronin, LLCEagan, MN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Breg, Inc.Carlsbad, CA, United StatesSpecification developer0000api.fda.gov
Beocare Inc., HudsonHudson, NC, United StatesManufacturer0000api.fda.gov
Colowrap LLCChapel Hill, NC, United StatesSpecification developer0000api.fda.gov
Columbus Canvas ProductsColumbus, OH, United StatesManufacturer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Core Products International IncChetek, WI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Dale Medical Products, Inc.New London, CT, United StatesManufacturer0000api.fda.gov
Darco International, Inc.Huntington, WV, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Djo, LLCCarlsbad, CA, United StatesSpecification developer0000api.fda.gov
Elastic Therapy, LLCAsheboro, NC, United StatesSpecification developer0000api.fda.gov
Frank StubbsOxnard, CA, United StatesManufacturer0000api.fda.gov
Golda, Inc.Beachwood, OH, United StatesSpecification developer0000api.fda.gov
Kenad SG Medical, Inc.Bartlett, TN, United StatesManufacturer0000api.fda.gov
Kentron Health Care, Inc.Springfield, TN, United StatesManufacturer0000api.fda.gov
L&R Usa Inc.Milwaukee, WI, United StatesContract manufacturer, Specification developer0000api.fda.gov
La Pointique International Ltd.Seattle, WA, United StatesSpecification developer0000api.fda.gov
Medical Specialties, Inc.Wadesboro, NC, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
My True Image MFG.Richmond, CA, United StatesManufacturer0000api.fda.gov
NYOrthoBrooklyn, NY, United StatesManufacturer0000api.fda.gov
Oppo Medical, Inc.Seattle, WA, United StatesSpecification developer0000api.fda.gov
Pepper Medical, Inc.West Chester, PA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Professional Products, Inc.Defuniak Spgs, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Surgical Appliance Industries, Inc.Cincinnati, OH, United StatesManufacturer0000api.fda.gov
Top Shelf Manufacturing, LLCTracy, CA, United StatesManufacturer0000api.fda.gov
Thuasne, LLCManchester, NH, United StatesComplaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
United Surgical LLCLaotto, IN, United StatesSpecification developer0000api.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.