Is this your brand? Sign in to claim ownership.
Sign in to claim this brandNingbo Cooskin Stationery Co., Ltd.
US
Last updated May 30, 2026
What Ningbo Cooskin Stationery Co., Ltd. makes
The company manufactures water jet flossers, including multiple variants of the COOSKIN brand, designed for oral hygiene to remove plaque and debris between teeth.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company 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 Ningbo Cooskin Stationery Co., Ltd. manufacture?
Ningbo Cooskin Stationery Co., Ltd. specializes in water jet flossers, specifically under the COOSKIN brand. These devices are designed to improve oral hygiene by removing plaque and debris from between teeth using a stream of water. The company focuses exclusively on this category of dental care products.
Where is Ningbo Cooskin Stationery Co., Ltd. based?
The company is based in the United States. This location is relevant for regulatory compliance and distribution, as it aligns with the FDA’s jurisdiction over medical devices marketed in the U.S.
Which regulatory registries list the devices manufactured by Ningbo Cooskin Stationery Co., Ltd.?
The devices produced by Ningbo Cooskin Stationery Co., Ltd., including their COOSKIN water jet flossers, are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for authorized devices under U.S. regulatory oversight.
How are the devices manufactured by Ningbo Cooskin Stationery Co., Ltd. classified under FDA regulations?
The water jet flossers produced by Ningbo Cooskin Stationery Co., Ltd. fall under Class I classification according to FDA regulations. This classification applies to devices posing minimal risk, where general controls are sufficient to ensure safety and effectiveness. The classification is determined based on the device’s intended use and potential risk profile.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 525609612
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cooskin | C13 | FDA UDI | Class I | Active |
| Cooskin | C9 | FDA UDI | Class I | Active |
| Cooskin | C11 | FDA UDI | Class I | Active |
| Cooskin | C8 | FDA UDI | Class I | Active |
| Cooskin | C12 | FDA UDI | Class I | Active |
| Cooskin | C8-1 | FDA UDI | Class I | Unknown |
| Cooskin | P7 | FDA UDI | Class I | Active |
| Cooskin | C91 | FDA UDI | Class I | Active |
| Cooskin | C10S | FDA UDI | Class I | Active |
| Cooskin | P6 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.