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Sign in to claim this brandFOSHAN OUSIDUN PERSONAL CARE PRODUCTS CO., LTD
US
Last updated May 24, 2026
What FOSHAN OUSIDUN PERSONAL CARE PRODUCTS CO., LTD makes
The company manufactures dental devices designed to accelerate tooth-bleaching procedures, specifically the AHVTE unit. These devices are intended for use in professional dental settings to enhance the effectiveness of teeth whitening treatments.
The AHVTE unit falls under FDA Class I regulation and is 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 FOSHAN OUSIDUN PERSONAL CARE PRODUCTS CO., LTD manufacture?
FOSHAN OUSIDUN PERSONAL CARE PRODUCTS CO., LTD specializes in dental devices, specifically the AHVTE unit, which is designed to accelerate tooth-bleaching procedures. These devices are intended for use in professional dental settings to improve the efficiency of teeth whitening treatments.
Where is FOSHAN OUSIDUN PERSONAL CARE PRODUCTS CO., LTD based?
The company is based in the United States. This location is relevant for understanding regulatory oversight and compliance, as it aligns with FDA jurisdiction for medical devices marketed in the US.
How are the devices manufactured by FOSHAN OUSIDUN PERSONAL CARE PRODUCTS CO., LTD classified by regulatory authorities?
The AHVTE unit, the primary device produced by the company, is classified as a Class I medical device by the FDA. This classification typically applies to devices posing minimal potential risk, often involving low-risk procedures or devices with simple design and intended use.
Are the devices from FOSHAN OUSIDUN PERSONAL CARE PRODUCTS CO., LTD listed in any regulatory registries?
Yes, the AHVTE unit is listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency in the supply chain, allowing healthcare providers and regulators to verify device details, such as manufacturer information and compliance status.
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
- 700741935
Catalogue (14)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Ahvte | MYY07 | FDA UDI | Class I | Active |
| Ahvte | MYY03 | FDA UDI | Class I | Active |
| Ahvte | MDY-002 | FDA UDI | Class I | Active |
| Ahvte | MDY-003 | FDA UDI | Class I | Active |
| Ahvte | MYY11 | FDA UDI | Class I | Active |
| Ahvte | MYY01 | FDA UDI | Class I | Active |
| Ahvte | MDY-001 | FDA UDI | Class I | Active |
| Ahvte | MYY10 | FDA UDI | Class I | Active |
| Ahvte | MYY02 | FDA UDI | Class I | Active |
| Ahvte | MYY09 | FDA UDI | Class I | Active |
| Ahvte | MYY08 | FDA UDI | Class I | Active |
| Ahvte | MDY-MYY001 | FDA UDI | Class I | Active |
| Ahvte | MYY06 | FDA UDI | Class I | Active |
| Ahvte | MDY-004 | FDA UDI | Class I | Active |
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