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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 1 of 38
DeviceModel / ReferenceRegistriesClassStatus
Meridian Medical 4250
FDA UDI
Class IIActive
Probasics BS16GB
FDA UDI
Class IActive
Winner Evo Package 410-010
FDA UDI
Class IIUnknown
Probasics PBBT001
FDA UDI
Class IActive
Medical Science Products Private Label 203-482
FDA UDI
Class IIActive
Roscoe Medical GB1021
FDA UDI
Class IIActive
Roscoe Medical HUM-ROS6
FDA UDI
Class IIActive
HydraTherm HT-TU-CHS
FDA UDI
Class IActive
Pain Cakes TMF70004
FDA UDI
Class IActive
Apex 00031
FDA UDI
UActive
Ultrasound Accessories 410-115
FDA UDI
Class IIActive
Multistim 400-8782-10
FDA UDI
Class IIActive
HydraTherm G-441
FDA UDI
Class IActive
Probasics X1WC4DAM07
FDA UDI
Class IActive
Roscoe Medical DOG-TRU
FDA UDI
Class IIActive
HydraTherm HT-TU-HLF
FDA UDI
Class IActive
Roscoe Medical DQ9275W5
FDA UDI
Class IIActive
Tens 7000 DT6070
FDA UDI
Class IIActive
TruMedical Self-Adhesive Reusable Electrodes 710280-003
FDA UDI
Class IIUnknown
Lotion/Gel Warmer 201-790
FDA UDI
Class IActive
Probasics WC72820DE
FDA UDI
Class IActive
Probasics X1WC4DAM08
FDA UDI
Class IActive
Probasics WCT41816DS
FDA UDI
Class IActive
SuperStim Electrodes 400-853
FDA UDI
Class IIUnknown
ProMed Electrotherapy Electrodes 203-812
FDA UDI
Class IIActive
LSI Silver Self Adhesive, Disposable Electrodes 300-161
FDA UDI
Class IIUnknown
Karatrode 203-338
FDA UDI
Class IIUnknown
Winner Evo Package 410-012
FDA UDI
Class IIUnknown
Direct Supply DS-TENS3
FDA UDI
Class IIActive
Karatrode 203-343
FDA UDI
Class IIActive
SuperStim Electrodes 400-893
FDA UDI
Class IIActive
Carex FGR10300 0000
FDA UDI
Class IActive
Probasics X1WC-ADJ-18TB
FDA UDI
Class IActive
TheraTouch DQ8222
FDA UDI
Class IIActive
Roscoe Medical ILB-516S
FDA UDI
Class IIActive
Roscoe Medical CPM-SFS
FDA UDI
Class IIActive
Apex 70059BAHO
FDA UDI
Class IActive
Roscoe elecs EF1200TC2
FDA UDI
Class IIActive
MultiStim Electrodes 400-879
FDA UDI
Class IIUnknown
Ionto Plus Large, Box of 12 201-453
FDA UDI
Class IIUnknown
Adhesive Electrodes 202-454
FDA UDI
Class IIUnknown
Probasics WC31616DE
FDA UDI
Class IActive
LSI Silver Self Adhesive, Disposable Electrodes 203-836
FDA UDI
Class IIActive
EZ-Stick 201-137
FDA UDI
Class IIUnknown
HydraTherm HT-PAT-SW120
FDA UDI
Class IActive
ScripHessco Basic Electrode 672 0192
FDA UDI
Class IIUnknown
Probasics WC3L1616DS
FDA UDI
Class IActive
Carex Health Brands HDC-9B 18X18
FDA UDI
Class IActive
MultiStim Electrodes 400-8611
FDA UDI
Class IIActive
BodyMed Iontophoresis Electrode Kit Small, Box of 12
FDA UDI
Class IIUnknown

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.