← Back to catalogue

Tne

FDA UDI

Class II (US FDA UDI)

by Temrex Corp.

Identity

Trade Name
TNE FDA UDI
Generic Name
Dental acrylic resin FDA UDI
Device Name
Resin Based Dental Cement FDA UDI
Model / Reference
7760 FDA UDI
Description
Resin Based Dental Cement FDA UDI

Identifiers

Primary DI / UDI-DI
00850015110054 FDA UDI
510(k) Number
K884081 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Dental acrylic resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3275 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

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 acrylic resin

Tne by Temrex Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental acrylic resin.

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
Temrex Corp.

Sources (1)

  • FDA UDI eeed006c-7108-4d95-aff9-f8020abe59b5 34 fields · synced May 30, 2026