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Sign in to claim this brandDr. Noze Best
US
Last updated May 27, 2026
What Dr. Noze Best makes
Dr. Noze Best manufactures electric nasal aspirators designed for infants and young children, including rechargeable and portable models. Their products include suction devices, disposable and reusable tubing, and replacement filters, as well as specialized attachments like newborn and standard nozepieces. These devices are intended for clearing nasal passages of mucus and debris in pediatric patients.
The company’s nasal aspirators are classified as Class II medical devices under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the United States, adhering to applicable regulatory standards for pediatric respiratory care devices.
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 Dr. Noze Best manufacture?
Dr. Noze Best specializes in electric nasal aspirators for infants and young children. These devices are designed to clear nasal passages of mucus and debris. Their product line includes rechargeable and portable models like the NozeBot and NozeBot On the Go, along with accessories such as disposable and reusable tubing, replacement filters, and specialized nozepieces (e.g., newborn and standard sizes).
Where is Dr. Noze Best based, and what region do their devices serve?
Dr. Noze Best is based in the United States. Their devices are intended for use in the U.S. market, where they comply with applicable regulatory standards for pediatric respiratory care products.
How are Dr. Noze Best’s devices classified under U.S. regulations?
Dr. Noze Best’s nasal aspirators fall under Class II medical device classification according to FDA regulations. This classification applies to devices that generally pose moderate risk and require special controls to ensure safety and effectiveness, such as electric suction devices for pediatric use.
Are Dr. Noze Best’s devices listed in any regulatory databases?
Yes, Dr. Noze Best’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and identify medical devices in the U.S., ensuring transparency and traceability for regulatory and market surveillance purposes.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- drnozebest.com
- —
- —
- [email protected]
- Phone
- 8664667668
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 080973698
Catalogue (12)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Snot Trap | DW-228500 | FDA UDI | Class II | Active |
| NozeBot | DW-228100 | FDA UDI | Class II | Active |
| Tubing | DW-228024 | FDA UDI | Class II | Active |
| NozeBot On the Go Nasal Aspirator | DW-229100 | FDA UDI | Class II | Active |
| Filters | DW-228400 | FDA UDI | Class II | Active |
| Newborn Nozepiece | DW-228032 | FDA UDI | Class II | Active |
| Saline Noze Mist | DW-230200 | FDA UDI | Class I | Unknown |
| Tubing | DW-228024 | FDA UDI | Class II | Active |
| Standard Nozepiece | DW-228200 | FDA UDI | Class II | Active |
| NozeBot | NNA2280 | FDA UDI | Class II | Active |
| Filters | DW-228400 | FDA UDI | Class II | Active |
| Standard Nozepiece | DW-228200 | FDA UDI | Class II | Active |
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