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Coxo

FDA UDI

Class I (US FDA UDI)

by Foshan COXO Medical Instrument Co., Ltd.

Identity

Trade Name
COXO FDA UDI
Generic Name
Dental surgical power tool motor, pneumatic FDA UDI
Device Name
High-Speed Air Turbine Handpieces FDA UDI
Model / Reference
CX207-G FDA UDI
Description
High-Speed Air Turbine Handpieces FDA UDI

Identifiers

Primary DI / UDI-DI
06974267891258 FDA UDI
510(k) Number
K220179 FDA UDI
FDA Product Code
EFB FDA UDI
EGS FDA UDI
GMDN Term
Dental surgical power tool motor, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical power tool motor, pneumatic

Coxo by Foshan COXO Medical Instrument Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical power tool motor, pneumatic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eae5dbe3-05e3-46f3-8b2f-8a8d69e204ac 34 fields · synced May 30, 2026