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Sign in to claim this brandMeret USA LLC
US
Last updated May 24, 2026
What Meret USA LLC makes
Meret USA LLC manufactures non-fixed medical gas cylinder regulators designed for controlling the flow of medical gases from portable or stationary cylinders. These devices include models with various pressure and flow rate settings, such as single-stage and multi-stage regulators, as well as specialized versions for emergency medical services and medical facility use.
The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These regulators are intended for use in healthcare settings, including hospitals, clinics, and emergency response environments, and comply with applicable U.S. regulatory requirements.
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 Meret USA LLC manufacture?
Meret USA LLC specializes in non-fixed medical gas cylinder regulators, which control the flow of medical gases from portable or stationary cylinders. These devices are designed for healthcare environments, including hospitals, clinics, and emergency medical services, ensuring precise gas delivery for patient care.
Where is Meret USA LLC based, and what regulatory regions do its devices serve?
Meret USA LLC is based in the United States. Its products are intended for the U.S. market and comply with applicable FDA regulations. The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, which helps track and identify medical devices under FDA oversight.
How are Meret USA LLC’s medical gas regulators classified under U.S. regulations?
Meret USA LLC’s non-fixed medical gas cylinder regulators are classified as Class I devices under FDA regulations. This classification applies to devices posing minimal risk to patients and users, typically requiring only general controls (e.g., good manufacturing practices) for compliance. The classification ensures these regulators meet basic safety and performance standards for medical gas delivery.
Which regulatory registries or databases list Meret USA LLC’s devices?
Meret USA LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, a centralized system that assigns a unique identifier to medical devices to improve tracking, transparency, and regulatory oversight. This listing helps healthcare providers and regulators verify the identity and compliance status of the company’s regulators.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- meretusa.com
- —
- —
- [email protected]
- Phone
- 949.502.3210
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 118070352
Catalogue (11)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Areg8715-Bu | AREG8715-BU | FDA UDI | Class I | Active |
| Areg8715me-Bu | AREG8715ME-BU | FDA UDI | Class I | Active |
| Prereg54-2d | PREREG54-2D | FDA UDI | Class I | Active |
| Emsmreg8725-B2d | EMSMREG8725-B2D | FDA UDI | Class I | Active |
| Mfmc-25 | MFMC-25 | FDA UDI | Class I | Active |
| Emsreg8725 | EMSREG8725 | FDA UDI | Class I | Active |
| Emsreg8725-B2d | EMSREG8725-B2D | FDA UDI | Class I | Active |
| Emsreg8725-B2d-Btm | EMSREG8725-B2D-BTM | FDA UDI | Class I | Active |
| Emsreg8725-B1d | EMSREG8725-B1D | FDA UDI | Class I | Active |
| Areg8725-B2d-Bu | AREG8725-B2D-BU | FDA UDI | Class I | Active |
| Areg8725-B2d-Bu-Knob | AREG8725-B2D-BU-KNOB | FDA UDI | Class I | Active |
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