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Data / Medical devices / Cushion, Flotation / United States

FDA-registered makers of Cushion, Flotation in the United States: 28 establishments

28 establishments in the United States are registered with the FDA to make Cushion, Flotation (product code KIC). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Get makers of this device in the United StatesWatch these makers
Device
Cushion, Flotation
Product code
KIC
Country
United States

Makers of Cushion, Flotation in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Action Products, Inc.Hagerstown, MD, United StatesManufacturer0000api.fda.gov
Addto, Inc.Elgin, IL, United StatesSpecification developer0000api.fda.gov
Alimed, LLCDedham, MA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Agiliti Health - CoronaCorona, CA, United StatesManufacturer0000api.fda.gov
Agiliti Health - EllisEllis, KS, United StatesManufacturer0000api.fda.gov
Breg, Inc.Carlsbad, CA, United StatesSpecification developer0000api.fda.gov
Comro Products, LLCDupo, IL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Cascade Designs Nevada, Inc.Reno, NV, United StatesManufacturer0000api.fda.gov
Dielectrics, Inc.Chicopee, MA, United StatesContract manufacturer0000api.fda.gov
Ehob, Inc.Indianapolis, IN, United StatesManufacturer0000api.fda.gov
Flocast LLC.Dolgeville, NY, United StatesManufacturer0000api.fda.gov
GF Health Products, IncAtlanta, GA, United StatesManufacturer0000api.fda.gov
K2 Health ProductsBrooklyn, NY, United StatesSpecification developer0000api.fda.gov
Ki MobilityStevens Point, WI, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Numotech, Inc.Northridge, CA, United StatesSpecification developer0000api.fda.gov
P.C.P. ChampionRipley, OH, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Professional Specialties Co., Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Purple Innovation, LLCMc Donough, GA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
ROHO, Inc.Belleville, IL, United StatesComplaint file establishment, Manufacturer0010api.fda.gov
Skil-Care Corp.New Rochelle, NY, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Stryker MedicalPortage, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Sunrise Medical (us) LLCFresno, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Sunrise Medical (US) LLCMount Juliet, TN, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
The Soule CoLutz, FL, United StatesManufacturer0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Vinyl Technology, Inc.Monrovia, CA, United StatesContract manufacturer0000api.fda.gov
WCW,IncManchester Center, VT, United StatesContract manufacturer, Manufacturer0000api.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.