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NuSmile BioFlx Cuspid Replacement Crown - Cuspid

FDA UDI

Class I (US FDA UDI)

by Nusmile, Ltd

Identity

Trade Name
NuSmile BioFlx Cuspid Replacement Crown - Cuspid FDA UDI
Generic Name
Preformed dental crown, temporary FDA UDI
Device Name
NuSmile BioFlx Cuspid Replacement Crown - Cuspid, Size 0 - Right / Light Shade FDA UDI
Model / Reference
C0R404L FDA UDI
Description
NuSmile BioFlx Cuspid Replacement Crown - Cuspid, Size 0 - Right / Light Shade FDA UDI

Identifiers

Primary DI / UDI-DI
00810118101663 FDA UDI
FDA Product Code
ELZ FDA UDI
GMDN Term
Preformed dental crown, temporary FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3330 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

NuSmile BioFlx Cuspid Replacement Crown - Cuspid by Nusmile, Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nusmile, Ltd

Sources (1)

  • FDA UDI 99b66660-e7dd-4a80-9a69-bc77c014180a 35 fields · synced May 31, 2026