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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 2 of 38
DeviceModel / ReferenceRegistriesClassStatus
Carex Health Brands ER2743B2
FDA UDI
Class IIActive
Reliable Medical E1F2020BC2-TU
FDA UDI
Class IIActive
TruMedical Self-Adhesive Reusable Electrodes 710281-001
FDA UDI
Class IIActive
Apex 70068GNP
FDA UDI
Class IActive
Stick-E-Pads 203-675
FDA UDI
Class IIActive
Meridian Medical / Leika 3102M-L
FDA UDI
Class IIUnknown
Probasics WKSAN2B
FDA UDI
Class IActive
Probasics WC4DX1816CE
FDA UDI
Class IActive
Roscoe 90611
FDA UDI
Class IActive
Meridian SGU_FG
FDA UDI
Class IActive
Therasound Evo Package 410-020
FDA UDI
Class IIUnknown
Roscoe ULTRA-5
FDA UDI
Class IIUnknown
World Wide Medical DI1010-WWM
FDA UDI
Class IIActive
Ecostim ECO2X3.5F
FDA UDI
Class IIActive
Stick-E-Pads 203-676
FDA UDI
Class IIUnknown
UltraStick - HJ & Associates PL 203-814
FDA UDI
Class IIActive
HydraTherm HT-TU-HBW
FDA UDI
Class IActive
Roscoe Medical GB1017
FDA UDI
Class IIActive
Roscoe Medical TENS-2000BN
FDA UDI
Class IIActive
PMI Probasics® HBSMX
FDA UDI
Class IIUnknown
Probasics X1WC4DAM13
FDA UDI
Class IActive
Probasics RLAH08SH
FDA UDI
Class IActive
Richmar EMG-RLW
FDA UDI
Class IIActive
Probasics RLEU10BK-SXR
FDA UDI
Class IActive
InTENSity DI2717
FDA UDI
Class IIActive
Probasics WC32016DE-2
FDA UDI
Class IActive
Adhesive Electrodes 202-674
FDA UDI
Class IIUnknown
Roscoe 90609
FDA UDI
Class IActive
Probasics TCA191612BK
FDA UDI
Class IActive
HydraTherm HT-TU-SHFKIT
FDA UDI
Class IActive
GelShot GSA5CH1
FDA UDI
Class IIUnknown
Apex 70060BPKG
FDA UDI
Class IActive
ScripHessco 672-5006-CH
FDA UDI
Class IIActive
ScripHessco 672 0023
FDA UDI
Class IIActive
Winner Evo Package 410-010
FDA UDI
Class IIUnknown
Roscoe RMI-04H
FDA UDI
Class IActive
Meridian Medical 4840-42-M
FDA UDI
Class IIActive
Therasound Evo Package 410-020-220
FDA UDI
Class IIUnknown
TENS Pros TP-GE2035TC
FDA UDI
Class IIActive
Roscoe Medical 50038
FDA UDI
Class IIActive
SuperStim Electrodes 400-857
FDA UDI
Class IIUnknown
Stick-E-Pads 203-682
FDA UDI
Class IIUnknown
MultiStim Electrodes 400-877
FDA UDI
Class IIActive
Roscoe 90089
FDA UDI
Class IActive
GelShot GSA5MT1
FDA UDI
Class IIUnknown
Panacea DS-APP2
FDA UDI
Class IIActive
LSI Silver Self Adhesive, Disposable Electrodes 203-566
FDA UDI
Class IIActive
Carex Health Brands FGA58100 0000
FDA UDI
Class IActive
Ionto Plus Butterfly, Box of 12 201-452
FDA UDI
Class IIUnknown
Richmar EP15140WF2
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.