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NuSmile BioFlx Permanent Molar Replacement Crown

FDA UDI

Class I (US FDA UDI)

by Nusmile, Ltd

Identity

Trade Name
NuSmile BioFlx Permanent Molar Replacement Crown FDA UDI
Generic Name
Preformed dental crown, temporary FDA UDI
Device Name
NuSmile BioFlx Permanent Molar Replacement Crown - Mandibular Right, Size 7 / Light Shade FDA UDI
Model / Reference
Y6LR7450L FDA UDI
Description
NuSmile BioFlx Permanent Molar Replacement Crown - Mandibular Right, Size 7 / Light Shade FDA UDI

Identifiers

Primary DI / UDI-DI
00810118103018 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
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

Category: Preformed dental crown, temporary

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

Similar devices

Also classified as Preformed dental crown, temporary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nusmile, Ltd

Sources (1)

  • FDA UDI 87f69594-c1f3-4b29-99c7-a2b063d45bf2 34 fields · synced May 31, 2026