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Cicada

FDA UDI

Class I (US FDA UDI)

by Foshan Cicada Dental Instrument Co., Ltd.

Identity

Trade Name
CICADA FDA UDI
Generic Name
Dental dressing forceps, reusable FDA UDI
Device Name
Tweezers For Dental Use FDA UDI
Model / Reference
DT-JCQ-I FDA UDI
Description
Tweezers For Dental Use FDA UDI

Identifiers

Primary DI / UDI-DI
06974456210518 FDA UDI
FDA Product Code
KCX FDA UDI
GMDN Term
Dental dressing forceps, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.5360 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

Yes

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 dressing forceps, reusable

Cicada by Foshan Cicada Dental Instrument Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental dressing forceps, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 455f863e-446b-4621-a480-478a17554b37 33 fields · synced May 30, 2026