Identity
- Trade Name
- COXO FDA UDI
- Generic Name
- Dental surgical power tool motor, electric FDA UDI
- Device Name
- Dental Electrical Motors FDA UDI
- Model / Reference
- C-PUMA MASTER FDA UDI
- Description
- Dental Electrical Motors FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06974267891067 FDA UDI
- 510(k) Number
- K220831 FDA UDI
- FDA Product Code
- EBW FDA UDIKMW FDA UDIEGS FDA UDI
- GMDN Term
- Dental surgical power tool motor, electric FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 FDA UDI872.4120 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Dental surgical power tool motor, electric
Coxo by Foshan COXO Medical Instrument Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K220831 also covers:
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Foshan COXO Medical Instrument Co., Ltd.
Sources (1)
- FDA UDI 9c186500-27ae-499b-b9ed-708e04cc556a 34 fields · synced May 30, 2026