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Interval Ii Plus

FDA UDI

Class II (US FDA UDI)

by Temrex Corp.

Identity

Trade Name
INTERVAL II PLUS FDA UDI
Generic Name
Glass ionomer dental cement FDA UDI
Device Name
SELF-CURED DENTAL FILLING MATERIAL FDA UDI
Model / Reference
7555 Jar 18gm. FDA UDI
Description
SELF-CURED DENTAL FILLING MATERIAL FDA UDI

Identifiers

Primary DI / UDI-DI
00850015110351 FDA UDI
510(k) Number
K934184 FDA UDI
FDA Product Code
EMA FDA UDI
GMDN Term
Glass ionomer dental cement 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: Glass ionomer dental cement

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

Similar devices

Also classified as Glass ionomer dental cement.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Temrex Corp.

Sources (1)

  • FDA UDI c2e98ed3-4c73-4807-871c-b96b0810020f 34 fields · synced May 30, 2026