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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 4 of 38
DeviceModel / ReferenceRegistriesClassStatus
Carex Health Brands FGA58500 0000
FDA UDI
Class IActive
Ultrasound Accessories 410-176
FDA UDI
Class IIUnknown
MultiStim Electrodes 400-852
FDA UDI
Class IIActive
Carex Health Brands FGA51200 0000
FDA UDI
Class IActive
Carex Health Brands HDC-WC1816
FDA UDI
Class IActive
American National APMAN-8000-LPNPUPFP
FDA UDI
Class IIActive
Meridian Medical SLV-HL
FDA UDI
Class IIActive
Probasics WC72218DS
FDA UDI
Class IActive
Probasics RLAH08BW
FDA UDI
Class IActive
Carex Health Brands FGA51700 BRNZ
FDA UDI
Class IActive
Sure Fit 203-808
FDA UDI
Class IIActive
Karatrode 203-336
FDA UDI
Class IIUnknown
Roscoe Medical APM-TLAL
FDA UDI
Class IIActive
Apex 00014
FDA UDI
UActive
Roscoe Medical TENS-6000BN
FDA UDI
Class IIActive
Winner Evo Package 410-012-220
FDA UDI
Class IIUnknown
Probasics WKAAW2B
FDA UDI
Class IActive
Richmar Rex - Universal DVTREX-U
FDA UDI
Class IIActive
Direct Supply DS8ROLL
FDA UDI
Class IActive
Carex Health Brands FGA51600 GRN
FDA UDI
Class IActive
Carex Health Brands CCFMEDUL100
FDA UDI
Class IActive
Probasics WC4L1616DS
FDA UDI
Class IUnknown
Probasics X1WC4DAM21
FDA UDI
Class IActive
Mpo DS9527
FDA UDI
Class IIActive
Winner Evo Package 410-012
FDA UDI
Class IIUnknown
Karatrode 203-340
FDA UDI
Class IIActive
LSI Silver Self Adhesive, Disposable Electrodes 300-174
FDA UDI
Class IIUnknown
Carex Health Brands FGR41500 0000
FDA UDI
Class IIActive
Probasics RLEU10PK
FDA UDI
Class IActive
PMI Probasics® 3170
FDA UDI
Class IIUnknown
SuperStim Electrodes 400-899
FDA UDI
Class IIUnknown
Probasics BSTF
FDA UDI
Class IActive
Roscoe Medical SIERRA-TRU
FDA UDI
Class IIActive
Carex Health Brands HDC-CX1816
FDA UDI
Class IActive
Reliable Medical E1F1515TC2-TU
FDA UDI
Class IIActive
MultiStim Electrodes 400-873
FDA UDI
Class IIActive
ScripHessco Basic Electrode EP84305C
FDA UDI
Class IIActive
LSI Silver Self Adhesive, Disposable Electrodes 300-170
FDA UDI
Class IIUnknown
Meridian X1SAPM201
FDA UDI
Class IIActive
HydraTherm HT-TU-CNVKIT
FDA UDI
Class IActive
Carex Health Brands FGA337C0 0000
FDA UDI
Class IActive
Direct Supply DS-ULTRSND
FDA UDI
Class IIActive
HydraTherm HT-TU-ELE010
FDA UDI
Class IActive
Multistim 400-8772-10
FDA UDI
Class IIActive
Roscoe EASY-FLEX6
FDA UDI
Class IActive
Apex 70036
FDA UDI
Class IActive
HydraTherm HT-TU-CNTRLPNLS
FDA UDI
Class IActive
ProMed Electrotherapy Electrodes 203-813
FDA UDI
Class IIActive
MultiStim Electrodes 400-872
FDA UDI
Class IIUnknown
Roscoe Medical IBF-RE
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.