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Creation Willi Geller

FDA UDI

Class II (US FDA UDI)

by KLEMA Dentalprodukte GmbH

Identity

Trade Name
Creation Willi Geller FDA UDI
Generic Name
Dental appliance fabrication material, ceramic FDA UDI
Device Name
LF/ Enamel E-58 FDA UDI
Model / Reference
302058 FDA UDI
Description
LF/ Enamel E-58 FDA UDI

Identifiers

Catalog Number
302058 FDA UDI
Primary DI / UDI-DI
ECWG3020581 FDA UDI
510(k) Number
K002904 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental appliance fabrication material, ceramic

Creation Willi Geller by KLEMA Dentalprodukte GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9d7a7522-cccc-442f-bec1-255e8828118d 36 fields · synced May 30, 2026