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COMPASS HEALTH BRANDS CORP.

US

Last updated May 24, 2026

What COMPASS HEALTH BRANDS CORP. makes

The company manufactures single-use transcutaneous electrical stimulation electrodes, reusable and reusable physical therapy systems for neuromuscular electrical stimulation, and reusable hot therapy packs for localized heating. It also produces non-bariatric push-rim manual wheelchairs, foldable handgrip disability-assistive walkers, alternating-pressure bed mattress overlays, soft-rubber chair cushions, and wheelchair seat cushions.

These products are classified under FDA’s Class I, Class II, and Unclassified (U) categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
—
LinkedIn
—
Facebook
—
Phone
800-376-7263
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
827221698

Catalogue (1863)

Page 7 of 38
DeviceModel / ReferenceRegistriesClassStatus
InTENSity EP2020WC2-INTM
FDA UDI
Class IIActive
Apex 60105QC
FDA UDI
Class IActive
Poly Stim II 203-482
FDA UDI
Class IIUnknown
MultiStim 2" x 3.5" Cloth 400-8792
FDA UDI
Class IIActive
Carex Health Brands FGR40300 0000
FDA UDI
Class IIActive
SuperStim Electrodes 400-8931
FDA UDI
Class IIActive
SuperStim Electrodes 400-8661
FDA UDI
Class IIActive
Bed Buddy BBF8009-12
FDA UDI
Class IActive
Ecostim ECO2X2C
FDA UDI
Class IIActive
GelShot GS902
FDA UDI
Class IIUnknown
Winner Evo Package 410-010
FDA UDI
Class IIUnknown
ScripHessco Standard Reusable Electrodes EP85848C
FDA UDI
Class IIActive
Winner Evo Package 410-010
FDA UDI
Class IIUnknown
Carex FGR10200 0000
FDA UDI
Class IActive
Winner Evo Package 410-012
FDA UDI
Class IIUnknown
Stratus 27300048
FDA UDI
Class IIActive
Probasics WC31816DE
FDA UDI
Class IActive
Probasics CRJ
FDA UDI
Class IActive
Pain Cakes TMF70005CA
FDA UDI
Class IActive
UltraStick 203-814
FDA UDI
Class IIUnknown
EZ-Stick 201-125
FDA UDI
Class IIUnknown
Roscoe X1DEF2HS04
FDA UDI
Class IActive
PMI Probasics® SA901P
FDA UDI
Class IIUnknown
Apex 70059BQC
FDA UDI
Class IActive
ScripHessco Silver Premium Electrodes 672 0194
FDA UDI
Class IIUnknown
Apt Performer 5100D038
FDA UDI
Class IActive
Apex 70059BGNP
FDA UDI
Class IActive
MultiStim Electrodes 400-8771
FDA UDI
Class IIActive
Probasics RLVXR10RG
FDA UDI
Class IActive
Roscoe DE7502
FDA UDI
Class IIActive
SuperStim Electrodes 400-866
FDA UDI
Class IIUnknown
Carex FGR10100 0000
FDA UDI
Class IActive
Therasound3 Standard 120V 410-026
FDA UDI
Class IIUnknown
Carex Health Brands CCFPS3020
FDA UDI
Class IActive
Roscoe Medical 70116
FDA UDI
Class IIActive
Winner Evo Package 410-012-220
FDA UDI
Class IIUnknown
PMI Probasics® Satin Air™ SA850K
FDA UDI
Class IIUnknown
Carex Health Brands HDC-CX2016
FDA UDI
Class IActive
Meridian Medical GEL-182
FDA UDI
Class IActive
Rite Aid 71021RA
FDA UDI
Class IIActive
HydraTherm HT-TU-ELBX
FDA UDI
Class IActive
MultiStim Electrodes 400-882
FDA UDI
Class IIActive
Roscoe Medical 50052
FDA UDI
Class IIUnknown
HydraTherm HT-R12-DR220
FDA UDI
Class IActive
Dex Trodes 202-291
FDA UDI
Class IIActive
LSI Silver Self Adhesive, Disposable Electrodes 300-159
FDA UDI
Class IIUnknown
Carex Health Brands FGA51000 0000
FDA UDI
Class IActive
Roscoe 90110
FDA UDI
Class IActive
StimChoice OTC Electrodes E20H-24A
FDA UDI
Class IIActive
Stratus 27300054
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Compass Health Brands Corp. has one recall record initiated on 2015-04-20, which is marked as terminated. The recall involved Roscoe Medical Nebulizers and was prompted by the need to update the user manual with additional warning statements regarding proper handling and storage.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Apr 20, 2015Z-1720-2015—terminated

Roscoe Medical has recently identified the need to update its user manual with additional warning statements regarding proper handling and storage of the nebulizer. These warnings are to better inform end users of proper care when using and storing a Roscoe Medical Nebulizer to reduce user damage (wear & tear) to the power cord.