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visio.lign system

FDA UDI

Class II (US FDA UDI)

by bredent GmbH & Co. KG

Identity

Trade Name
visio.lign system FDA UDI
Generic Name
Dental veneer, professional FDA UDI
Device Name
novo.lign P veneer posterior 2G3 upper A10 4 parts (24,25,26,27) 1 Assortment FDA UDI
Model / Reference
novo.lign FDA UDI
Description
novo.lign P veneer posterior 2G3 upper A10 4 parts (24,25,26,27) 1 Assortment FDA UDI

Identifiers

Catalog Number
VO2G3A10 FDA UDI
Primary DI / UDI-DI
VO2G3A10 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Dental veneer, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental veneer, professional

visio.lign system by bredent GmbH & Co. KG — Class II — 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

Manufacturer
bredent GmbH & Co. KG

Sources (1)

  • FDA UDI e684c1d3-237c-459f-941c-4dea29327f3c 36 fields · synced Jun 1, 2026