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Lava™ Esthetic

FDA UDI

Class II (US FDA UDI)

by 3M Deutschland GmbH

Identity

Trade Name
Lava™ Esthetic FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
3M™ ESPE™ Lava™ Esthetic Disc, 98S-18MM D2, 69334 FDA UDI
Model / Reference
69334 FDA UDI
Description
3M™ ESPE™ Lava™ Esthetic Disc, 98S-18MM D2, 69334 FDA UDI

Identifiers

Catalog Number
69334 FDA UDI
Primary DI / UDI-DI
J001702011454740 FDA UDI
FDA Product Code
EIH FDA UDI
GMDN Term
Dental appliance fabrication material, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6660 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

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 appliance fabrication material, ceramic

Lava™ Esthetic by 3M Deutschland GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
3M Deutschland GmbH

Sources (1)

  • FDA UDI 0598b7bd-d999-497e-86ca-7be21f46f095 35 fields · synced May 30, 2026