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Sign in to claim this brandSCOTTCARE CORPORATION, THE
US
Last updated May 24, 2026
What SCOTTCARE CORPORATION, THE makes
The company manufactures professional multichannel electrocardiographs, ambulatory ECG recorders, and related monitoring systems for cardiac assessment. Their portfolio includes long-term Holter monitoring devices, telemetric ECG transmitters and receivers, patient cables, and software for ECG data analysis and editing. These products are designed for continuous cardiac rhythm monitoring in clinical and remote settings, as well as telemetric transmission of ECG data for remote patient monitoring.
All listed devices fall under Class II regulatory classification in the US, with each product authorised through the FDA’s UDI (Unique Device Identification) system. The company’s portfolio is exclusively regulated under US jurisdiction, with no indications of international listings or additional regulatory pathways. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does ScottCare Corporation manufacture?
ScottCare Corporation specialises in cardiac monitoring devices. Their portfolio includes professional multichannel electrocardiographs, ambulatory ECG recorders (such as Holter monitors), telemetric ECG transmitters and receivers, patient cables, and software applications for ECG data analysis and editing. These products are designed for continuous cardiac rhythm monitoring in clinical settings or for remote patient assessment.
Where is ScottCare Corporation based, and does it operate internationally?
ScottCare Corporation is based in the United States. Their devices are exclusively regulated under US jurisdiction, specifically through the FDA’s UDI (Unique Device Identification) system. There are no indications that the company operates under additional regulatory pathways outside the US.
Which regulatory registries or databases list ScottCare Corporation’s devices?
ScottCare Corporation’s devices are listed in the FDA’s UDI (Unique Device Identification) system. This database is used to track and identify medical devices authorised for use in the US. The company’s products are not listed in international registries or databases.
How are ScottCare Corporation’s devices classified under US regulations?
All of ScottCare Corporation’s devices fall under Class II regulatory classification in the US. This classification applies to devices that generally pose moderate risk and require special controls to ensure their safety and effectiveness, such as cardiac monitoring systems and related software applications.
What is the primary purpose of ScottCare Corporation’s electrocardiography products?
ScottCare Corporation’s devices are designed for continuous cardiac assessment, including professional ECG monitoring, long-term Holter recording, and telemetric transmission of ECG data. Their products enable clinicians to track heart rhythms in clinical environments or remotely, supporting diagnostics for conditions like arrhythmias or other cardiac abnormalities.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- scottcare.com
- —
- —
- [email protected]
- Phone
- 216-362-0550
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 808204957
Catalogue (34)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| EZLink | EZLink | FDA UDI | Class II | Active |
| HolterCare Editing Kit | HolterCare Editing Kit | FDA UDI | Class II | Active |
| Chroma 5 Lead Patient Cable | 100605 | FDA UDI | Class II | Active |
| Chroma2 7 Lead Patient Cable | Chroma2 7 Lead Patient Cable | FDA UDI | Class II | Active |
| TeleSense/Chroma2 Download Cable | TeleSense/Chroma2 Download Cable | FDA UDI | Class II | Active |
| TeleSenseRCM | MCT1774 | FDA UDI | Class II | Active |
| TeleRehab Receiver Box | TR620 | FDA UDI | Class II | Active |
| TeleSentry Battery | TS01 | FDA UDI | Class II | Active |
| Chroma2 | RZ153C2 | FDA UDI | Class II | Active |
| EventCare | EventCare | FDA UDI | Class II | Active |
| TeleSense-E | E1774 | FDA UDI | Class II | Active |
| HolterCare | HolterCare | FDA UDI | Class II | Active |
| Chroma 7 Lead Patient Cable | 100608 | FDA UDI | Class II | Active |
| EZLink-C | EZLink-C | FDA UDI | Class II | Active |
| Chroma2 5 Lead Patient Cable | Chroma2 5 Lead Patient Cable | FDA UDI | Class II | Active |
| Telemetry 5 Lead Patient Cable | Telemetry 5 Lead Patient Cable | FDA UDI | Class II | Active |
| TeleRehab Computer | TeleRehab Computer | FDA UDI | Class II | Active |
| TeleRehab Software Work Station/Seat License | TeleRehab Software Work Station/Seat License | FDA UDI | Class II | Active |
| TeleSense 3 Lead Patient Cable 30" | TeleSense 3 Lead Patient Cable 30" | FDA UDI | Class II | Active |
| Angel | DS2 | FDA UDI | Class II | Active |
| Chroma | RZ153C | FDA UDI | Class II | Active |
| OneView | OneView | FDA UDI | Class II | Active |
| Transtelephonic Receiving Module | Transtelephonic Receiving Module | FDA UDI | Class II | Active |
| TeleSense Software | TeleSense Software | FDA UDI | Class II | Active |
| Novi Software | Novi Software | FDA UDI | Class II | Active |
| Innovo | Innovo | FDA UDI | Class II | Active |
| TeleRehab Receiver Card | TeleRehab Receiver Card | FDA UDI | Class II | Active |
| ABPCare | ABPCare | FDA UDI | Class II | Active |
| TeleRehab Rack Server | TeleRehab Rack Server | FDA UDI | Class II | Active |
| TeleRehab Software File Manager | TeleRehab Software File Manager | FDA UDI | Class II | Active |
| EZLink-R | EZLink-R | FDA UDI | Class II | Active |
| TeleSentry 3 Lead Patient Cable | TeleSentry 3 Lead Patient Cable | FDA UDI | Class II | Active |
| Telemetry 3 Lead Patient Cable | Telemetry 3 Lead Patient Cable | FDA UDI | Class II | Active |
| TeleSense 3 Lead Patient Cable 40" | TeleSense 3 Lead Patient Cable 40" | FDA UDI | Class II | Active |
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