Skip to the page
Get started free

Data / Medical devices / Sleeve, Limb, Compressible / United States

FDA-registered makers of Sleeve, Limb, Compressible in the United States: 47 establishments

47 establishments in the United States are registered with the FDA to make Sleeve, Limb, Compressible (product code JOW). 37 have a 510(k) clearance or PMA approval on file and 4 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
Sleeve, Limb, Compressible
Product code
JOW
Country
United States

Makers of Sleeve, Limb, Compressible in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Airos Medical IncAudubon, PA, United StatesManufacturer, Specification developer12October 11, 2024000api.fda.gov
Bio Compression Systems, Inc.Moonachie, NJ, United StatesManufacturer12September 11, 2026000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer11April 3, 2023000api.fda.gov
Djo, LLCCarlsbad, CA, United StatesComplaint file establishment, Specification developer11January 21, 2021000api.fda.gov
Currie Medical, Inc.Franklin, TN, United StatesRemanufacturer, Reprocessor, Specification developer8December 10, 2015000api.fda.gov
Zimmer Surgical, Inc.Dover, OH, United StatesManufacturer, Specification developer7July 16, 2015000api.fda.gov
KL DistributingHudson, FL, United StatesManufacturer6January 20, 2023000api.fda.gov
Precision Medical ProductsRocklin, CA, United StatesSpecification developer5June 3, 2022010api.fda.gov
Renu Medical, Inc.Everett, WA, United StatesComplaint file establishment, Repackager or relabeler, Reprocessor5May 7, 2021000api.fda.gov
Cardinal HealthRiverview, FL, United StatesManufacturer, Reprocessor4April 3, 2023000api.fda.gov
Manamed LLCDenton, TX, United StatesSpecification developer4September 17, 2025000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesComplaint file establishment, Specification developer4September 8, 2017000api.fda.gov
Tactile Systems Technology IncNew Brighton, MN, United StatesManufacturer4June 21, 2024000api.fda.gov
Aci Medical, LLCSan Marcos, CA, United StatesManufacturer3February 10, 2014000api.fda.gov
Djo, LLCVista, CA, United StatesManufacturer3October 18, 2012020api.fda.gov
Normatec Industries, LPWatertown, MA, United StatesSpecification developer3December 21, 2018000api.fda.gov
Sun-Scientific Inc.Dobbs Ferry, NY, United StatesManufacturer, Repackager or relabeler, Specification developer3September 7, 2023000api.fda.gov
Stryker Sustainability SolutionsTempe, AZ, United StatesReprocessor, Specification developer3July 23, 2010030api.fda.gov
VQ OrthocareVista, CA, United StatesRepackager or relabeler, Specification developer3April 1, 2016000api.fda.gov
Breg, Inc.Carlsbad, CA, United StatesRepackager or relabeler, Specification developer2January 21, 2021000api.fda.gov
Compression Solutions, LLCCharlotte, NC, United StatesSpecification developer2June 12, 2014000api.fda.gov
Koya Medical, Inc.Dallas, TX, United StatesComplaint file establishment, Manufacturer2April 23, 2021000api.fda.gov
Medi Usa, LPWhitsett, NC, United StatesSpecification developer2July 7, 2022000api.fda.gov
Medline ReNewalRedmond, OR, United StatesReprocessor2January 16, 2015010api.fda.gov
Pulsar Scientific, LLCLudlow, MA, United StatesManufacturer, Specification developer2April 2, 2021000api.fda.gov
Secured Ortho Manufacturing Of America, LLCDeer Park, NY, United StatesSpecification developer2June 20, 2013000api.fda.gov
Thermotek, Inc.Flower Mound, TX, United StatesManufacturer, Specification developer2December 10, 2010000api.fda.gov
Biotab LLCSaint Louis, MO, United StatesManufacturer, Specification developer1August 18, 2025000api.fda.gov
Currie Medical, Inc.Norfolk, VA, United StatesSpecification developer1December 14, 2023000api.fda.gov
Hanuri Distribution, IncChatsworth, CA, United StatesManufacturer1November 9, 2011000api.fda.gov
Midway MedicalBloomington, IL, United StatesSpecification developer1July 22, 2019000api.fda.gov
Microtek Medical LLCNorthfield, IL, United StatesSpecification developer1October 25, 2001000api.fda.gov
Recovery Force HealthFishers, IN, United StatesManufacturer1March 21, 2021000api.fda.gov
Stryker Sustainability Solutions - ChandlerChandler, AZ, United StatesReprocessor1July 23, 2010000api.fda.gov
United Medical Resources LLCN Salt Lake, UT, United StatesReprocessor1February 12, 2014000api.fda.gov
VIVE Health LLCNaples, FL, United StatesSpecification developer1August 8, 2025000api.fda.gov
Zenith Technical Innovations, LLCGurnee, IL, United StatesManufacturer1June 21, 2024000api.fda.gov
AJR Specialty Products, LLCSaint Charles, IL, United StatesContract manufacturer0000api.fda.gov
Albert International, Inc.Gainesville, GA, United StatesContract manufacturer0000api.fda.gov
Alleva Medical DevicesPomona, CA, United StatesContract manufacturer0000api.fda.gov
Clearlake-Tech IncClear Lake, SD, United StatesContract manufacturer0000api.fda.gov
Medi MFG., Inc.Whitsett, NC, United StatesContract manufacturer0000api.fda.gov
Nypro Inc (Maple Grove)Maple Grove, MN, United StatesContract manufacturer0000api.fda.gov
Plexus Corp.Buffalo Grove, IL, United StatesContract manufacturer0000api.fda.gov
Scientific Molding Corporation, Ltd. Dba SMC Ltd.Somerset, WI, United StatesContract manufacturer0000api.fda.gov
Vonco Products, LLCFortville, IN, United StatesContract manufacturer0000api.fda.gov
Zoll Medical CorporationChelmsford, MA, United StatesComplaint file establishment, Manufacturer, Specification 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.