← Back to catalogue

Silan-IT

FDA UDI

Class II (US FDA UDI)

by Itena Clinical

Identity

Trade Name
Silan-IT FDA UDI
Generic Name
Dental prosthesis priming agent FDA UDI
Device Name
Cross-linking agent containing silan agent to improve adhesion FDA UDI
Model / Reference
SILAN-IT FDA UDI
Description
Cross-linking agent containing silan agent to improve adhesion FDA UDI

Identifiers

Primary DI / UDI-DI
03760260223119 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dental prosthesis priming agent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 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 prosthesis priming agent

Silan-IT by Itena Clinical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis priming agent.

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
Itena Clinical

Sources (1)

  • FDA UDI 49e79975-b344-4689-b280-1ec2f1b52573 35 fields · synced May 30, 2026