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Tokuyama Universal Bond II

FDA UDI

Class II (US FDA UDI)

by Tokuyama Dental Corporation

Identity

Trade Name
Tokuyama Universal Bond II FDA UDI
Generic Name
Dentine bonding agent/set FDA UDI
Device Name
Kit FDA UDI
Model / Reference
15310 FDA UDI
Description
Kit FDA UDI

Identifiers

Primary DI / UDI-DI
04548190153107 FDA UDI
510(k) Number
K203760 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dentine bonding agent/set 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

Yes

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: Dentine bonding agent/set

Tokuyama Universal Bond II by Tokuyama Dental Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentine bonding agent/set.

Cleared under the same submission

K203760 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tokuyama Dental Corporation

Sources (1)

  • FDA UDI 03edf536-61f9-46cd-a9b4-abfe25583e79 36 fields · synced May 30, 2026