← Back to catalogue

Nobilium

FDA UDI

Class II (US FDA UDI)

by Cmp Industries Llc

Identity

Trade Name
Nobilium FDA UDI
Generic Name
Composite dental impression material FDA UDI
Device Name
GENERAL PURPOSE DENTAL TRAY FDA UDI
Model / Reference
689LT123N FDA UDI
Description
GENERAL PURPOSE DENTAL TRAY FDA UDI

Identifiers

Primary DI / UDI-DI
M482689LT123N1 FDA UDI
510(k) Number
K133071 FDA UDI
FDA Product Code
ELW FDA UDI
GMDN Term
Composite dental impression material FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3660 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Composite dental impression material

Nobilium by Cmp Industries Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Composite dental impression material.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cmp Industries Llc

Sources (1)

  • FDA UDI 679867ba-3b07-4e4d-9cec-2bacfb6b1e34 34 fields · synced Jun 6, 2026