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Ultrathineer

FDA UDI

Class N (US FDA UDI)

by BMF Tech (Zhuhai) Inc.

Identity

Trade Name
ULTRATHINEER FDA UDI
Generic Name
Dental veneer, professional FDA UDI
Model / Reference
Zirconia veneer FDA UDI

Identifiers

Primary DI / UDI-DI
06977053950054 FDA UDI
FDA Product Code
NSP FDA UDI
GMDN Term
Dental veneer, professional FDA UDI

Classification

Device Class
N 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

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental veneer, professional

Ultrathineer by BMF Tech (Zhuhai) Inc. — Class N — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental veneer, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a342aeec-7586-432e-a180-ee8130bb4bd0 32 fields · synced May 30, 2026