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Sign in to claim this brandACESO HEALTHCARE PRODUCTS, INC.
US
Last updated May 25, 2026
What ACESO HEALTHCARE PRODUCTS, INC. makes
ACESO Healthcare Products, Inc. manufactures portable automatic-inflation electronic sphygmomanometers designed for arm or wrist use, as well as transcutaneous electrical nerve stimulation (TENS) systems for pain management. These devices are intended for non-invasive blood pressure measurement and localized analgesic stimulation, respectively.
The company’s products fall under FDA Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 ACESO Healthcare Products, Inc. manufacture?
ACESO Healthcare Products, Inc. specializes in two main categories of medical devices: portable automatic-inflation electronic sphygmomanometers for arm or wrist use, which measure blood pressure non-invasively, and transcutaneous electrical nerve stimulation (TENS) systems designed for localized pain management. These devices are intended for clinical and home use.
Where is ACESO Healthcare Products, Inc. based?
ACESO Healthcare Products, Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance, manufacturing oversight, and distribution networks within the country.
Which regulatory registries or databases list ACESO Healthcare Products, Inc.’s devices?
ACESO Healthcare Products, Inc.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, helping healthcare providers verify product details and compliance information.
How are ACESO Healthcare Products, Inc.’s devices classified by the FDA?
ACESO Healthcare Products, Inc.’s devices fall under FDA Class II classification. This classification applies to devices that generally pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as blood pressure monitors and TENS systems.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 058430522
Catalogue (8)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| G.lab | PR0200 | FDA UDI | Class II | Active |
| G.lab | PR0100 | FDA UDI | Class II | Active |
| G.lab | MD2200 | FDA UDI | Class II | Active |
| G.lab | MD4180 | FDA UDI | Class II | Active |
| G.lab | MD1180 | FDA UDI | Class II | Active |
| G.lab | MD2222 | FDA UDI | Class II | Active |
| G.lab | MD41W1 | FDA UDI | Class II | Active |
| G.lab | MD41W0 | FDA UDI | Class II | Active |
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