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Sign in to claim this brandCOMPASS 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
- —
- Website
- compasshealthbrands.com
- —
- —
- [email protected]
- Phone
- 800-376-7263
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 827221698
Catalogue (1863)
Page 5 of 38| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bed Buddy | BBF5085-12 | FDA UDI | Class I | Active |
| GelShot | GSA10RM1 | FDA UDI | Class II | Unknown |
| Ionto Plus Butterfly 2.0 cc | 201-439 | FDA UDI | Class II | Active |
| Probasics | WKABN2B | FDA UDI | Class I | Active |
| MicroBlock Antimicrobial Electrode | 400-852-MIC | FDA UDI | Class II | Active |
| Roscoe Medical | EP4000RR7 | FDA UDI | Class II | Active |
| PMI Probasics® Satin Air™ | APMBARI48 | FDA UDI | Class II | Unknown |
| Meridian | #6003S | FDA UDI | Class II | Unknown |
| Reliable Medical | E1P2035WC2-TU | FDA UDI | Class II | Active |
| Probasics | RLASXRCB | FDA UDI | Class I | Active |
| Viverity | E101-6R | FDA UDI | Class II | Active |
| GelShot | GS901 | FDA UDI | Class II | Unknown |
| EZ-Stick | 201-154 | FDA UDI | Class II | Active |
| Roscoe | X1GOSH02 | FDA UDI | Class I | Active |
| UltraStick | 203-815 | FDA UDI | Class II | Unknown |
| TENS Pros | TP-GE2020TC | FDA UDI | Class II | Active |
| Probasics | WC12016DE | FDA UDI | Class I | Active |
| Therasound EVO 3.5P | 400-020 | FDA UDI | Class II | Unknown |
| Probasics | X1WC4DAM20 | FDA UDI | Class I | Active |
| Tens 7000 Conductive Sleeves | DT7202-SLEEVE | FDA UDI | Class II | Active |
| Roscoe | WCBF-2283 | FDA UDI | Class I | Active |
| Roscoe Medical | E1F1515TC2 | FDA UDI | Class II | Active |
| MultiStim 3" x 5", Cloth | 400-8522 | FDA UDI | Class II | Active |
| Stratus | 27300056 | FDA UDI | Class II | Active |
| HydraTherm | G-522 | FDA UDI | Class I | Active |
| HydraTherm | HT-PAU-DW220 | FDA UDI | Class I | Active |
| BodyMed Iontophoresis Electrode Kit | Medium (3.25"x3.25") | FDA UDI | Class II | Unknown |
| EZ-Stick | 201-130 | FDA UDI | Class II | Active |
| Roscoe | WCF-203 | FDA UDI | Class I | Active |
| Optimum Gel Wheelchair Cushion - 22 x 18 x 3 | HDC-9B 22X18 | FDA UDI | Class I | Active |
| Roscoe | ADLT-MASK | FDA UDI | Class I | Active |
| MultiStim Electrodes | 400-8511 | FDA UDI | Class II | Active |
| Roscoe Medical | DT4444 | FDA UDI | Class II | Active |
| AccuRelief | ACRL-9001 | FDA UDI | Class II | Active |
| HydraTherm | HT-R12-DRW220 | FDA UDI | Class I | Active |
| American Bantex | 90086 | FDA UDI | Class II | Active |
| Winner Evo Package | 410-012 | FDA UDI | Class II | Unknown |
| Meridian | 4530_1816 | FDA UDI | Class II | Active |
| MultStim 2" x 2" Cloth | 400-8772 | FDA UDI | Class II | Active |
| Carex Health Brands | ER2535B2 | FDA UDI | Class II | Active |
| MultiStim Electrodes | 400-8621 | FDA UDI | Class II | Active |
| TruMedical Self-Adhesive Reusable Electrodes | 710280-002 | FDA UDI | Class II | Unknown |
| Roscoe Medical | CPF-DSR1 | FDA UDI | Class II | Active |
| American National | APMAN-8000S-LPNPUPFP | FDA UDI | Class II | Active |
| BodyMed Iontophoresis Electrode Kit | Butterfly (3.75"x3.75") | FDA UDI | Class II | Unknown |
| Mpo | DT7259 | FDA UDI | Class II | Active |
| Apex | 70054 | FDA UDI | Class I | Active |
| Roscoe Medical | DT4222 | FDA UDI | Class II | Active |
| Apex | 61919 | FDA UDI | Class I | Active |
| Mpo | DE7529 | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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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.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Apr 20, 2015 | Z-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. |