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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 6 of 38
DeviceModel / ReferenceRegistriesClassStatus
Carex Health Brands HDC-WC1616
FDA UDI
Class IActive
PMI Probasics® 8011
FDA UDI
Class IIUnknown
Probasics CNOFHD
FDA UDI
Class IActive
Carex Health Brands FGR11000 0000
FDA UDI
Class IIActive
Roscoe Medical 196472-14
FDA UDI
Class IIActive
InTENSity 7 DI0007
FDA UDI
Class IIActive
Carex Health Brands FGA50700 0000
FDA UDI
Class IActive
EZ-Stick 201-126
FDA UDI
Class IIActive
AccuRelief ACRL-9100CA
FDA UDI
Class IIActive
Ecostim ECO3RF
FDA UDI
Class IIActive
Stick-E-Pads 203-679
FDA UDI
Class IIActive
Probasics WC31616DS
FDA UDI
Class IActive
Probasics WC12016DS
FDA UDI
Class IActive
Meridian Medical SLV-FLS
FDA UDI
Class IIActive
Roscoe Medical SMB-HBFB
FDA UDI
Class IIUnknown
Probasics WC32016DS-2
FDA UDI
Class IActive
Roscoe Medical CPF-PR1
FDA UDI
Class IIActive
Roscoe Medical EP1525WR2
FDA UDI
Class IIActive
Therasound 410-029
FDA UDI
Class IIUnknown
Winner Evo Package 410-012-220
FDA UDI
Class IIUnknown
Richmar TwinStim DS2202
FDA UDI
Class IIActive
InTENSity DQ8000
FDA UDI
Class IIUnknown
Probasics WC72418DE
FDA UDI
Class IActive
InTENSity DI3717
FDA UDI
Class IIActive
Roscoe Medical TK-SUC4
FDA UDI
Class IIActive
LG Med Supply DT3039
FDA UDI
Class IIActive
Roscoe Medical 3201
FDA UDI
Class IIUnknown
HydraTherm HT-TU-BAG
FDA UDI
Class IActive
Apex 70085QC
FDA UDI
Class IActive
UltraStick 203-816
FDA UDI
Class IIUnknown
Carex Health Brands FGA56400 0000
FDA UDI
Class IActive
EZ-Stick 201-123
FDA UDI
Class IIUnknown
LG Med Supply DC8420
FDA UDI
Class IIActive
HydraTherm HT-R12-S220
FDA UDI
Class IActive
ScripHessco Standard Reusable Electrodes 672 0010
FDA UDI
Class IIUnknown
Roscoe Medical 50004
FDA UDI
Class IIActive
HydraTherm HT-PAT-DRW120
FDA UDI
Class IActive
MultiStim Electrodes 400-880
FDA UDI
Class IIUnknown
Roscoe Medical CPF-S9PK2
FDA UDI
Class IIActive
Roscoe EASY-FLEX8
FDA UDI
Class IActive
GelShot GSA2RM1
FDA UDI
Class IIUnknown
Roscoe Medical ASP-ROSP
FDA UDI
Class IIActive
Carex FGR41800 0000
FDA UDI
Class IIActive
Roscoe Medical DQ8450
FDA UDI
Class IIActive
Poly Stim II 203-484
FDA UDI
Class IIUnknown
UltraStick 203-818
FDA UDI
Class IIUnknown
Tens 7000 Conductive Socks DT7202-SOCK
FDA UDI
Class IIActive
Roscoe Medical CPM-DEFS
FDA UDI
Class IIActive
LG Med Supply DC5700
FDA UDI
Class IIActive
Winner Evo Package 410-010-220
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.